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Author: Subject: Protocatechuic aldehyde from ethylvanillin
Diachrynic
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[*] posted on 17-3-2022 at 14:52
Protocatechuic aldehyde from ethylvanillin


Vanillin is notoriously hard to turn into protocatechuic aldehyde. Ethylvanillin, on the other hand, is much easier to dealkylate. While I haven't found a direct source, german patent DE69507676[5] uses a two step process to convert ethylvanillin into isovanillin, by methylation and then deethylation. I was curious if ethylvanillin itself could be turned into protocatechuic aldehyde this way.

Alternative names for protocatechuic aldehyde are protocatechualdehyde, 3,4-dihydroxybenzaldehyde or [139-85-5].

Chemicals:
Ethylvanillin
Sulfuric acid (95-97%, pure)
Ethyl acetate
Ice
Petrol ether (for TLC)
Glacial acetic acid (for TLC)
(Sodium sulfate)

Procedure:
In a 150 mL beaker were placed 5.5 g of concentrated sulfuric acid and a stirbar. Then 1 g of ethylvanillin was added and stirred in, the pieces take on a greenish color before dissolving to a clear yellow solution. The beaker is covered with a watch glass, placed in an oil bath in the fume hood, the temperature of the oil is raised to 70 °C and maintained for 4 hours. Some smoke or fog is visible in the beaker.

Reaction progress can be monitored by TLC: A glass rod is used to extract a drop of the acid which is dissolved in about 1 mL of water. This solution is spotted along a reference sample of ethylvanillin dissolved in ethanol onto a TLC plate. Eluent mixture is petrol ether/ethyl acetate 1/1 v/v with a few drops of glacial acetic acid added. (The Rf values are for 0.2 g per 10 mL eluent.) Staining is accomplished by 254 nm UV (quenching) or by staining with iodine vapor (more sensitive).

Rf (ethylvanillin) = 0.60
Rf (protocatechuic aldehyde) = 0.37

Samples were taken after 2, 3 and 4 hours. During this time the ethylvanillin spot gets weaker and weaker.

The reaction mixture that has taken on a brown color by now is taken out of the oil bath and left to cool for a moment before it is dumped onto 11 g of crushed ice while being stirred. A clear solution results. The mixture is almost fully molten but still cold. Then it is extracted once with 10 mL of ethyl acetate and then twice with 5 mL of ethyl acetate each. The color moves mostly into the organic layer (reddish). The organic layers are combined, dried over some sodium sulfate and then evaporated to about 2-3 mL volume which is allowed to evaporate at room temperature. Greyish crystals with a hint of blue and green are obtained and left to dry in air for half a day.
They weigh 0.77 g (93%).

pa_1.jpg - 122kB pa_2.jpg - 148kB pa_3.jpg - 178kB

The solids are redissolved in about 4.4 g of hot water, giving a brown solution. On cooling to room temperature crystallisation had to be initiated by scraping with a spatula. The suspension of crystals was then placed for several hours in the fridge. Vacuum filtration over a Büchner funnel provides a slightly brownish crystalline product.
After air drying it weighs 0.51 g (63%).

pa_4.jpg - 353kB

TLC (pet ether/ethyl acetate 1/1 v/v + a few drops of glacial acetic acid) shows a large spot at Rf = 0.37 and a faint spot at Rf = 0.60 (small amount of leftover ethylvanillin).

The melting point was measured to be between 149-151 °C. Ethylvanillin melts around 77 °C, the values for protocatechuic aldehyde range from 150 to 156 °C, depending on the source. Amarego lists 153 °C.[4]

Melting point and TLC thus give convincing evidence that ethylvanillin was successfully dealkylated.

Possible improvements:
The procedure should be carried out in an appropriately sized RBF to avoid the sulfuric acid absorbing moisture from the air. The reaction mixture should perhaps be stirred for longer. Alternatively, the temperature could probably be increased while the reaction time being decreased. The stirbar should be submerged because ethylvanillin can stick to it and not react.
The diluted solution could be extracted with more ethyl acetate.
Finally, less water should be used for the recrystallisation, and it could be cooled further in the freezer. It has also been suggested to recrystallise from toluene.[4]

The patent[5] uses a ratio of 2.7 g of sulfuric acid per gram of 3-ethoxy-4-methoxybenzaldehyde. On this scale I preferred ease of stirring and used a larger excess of acid, but it might not be required.

Drying the ethyl acetate with sodium sulfate is unnecessary if the product is recrystallised from water anyways.

[EDIT 18.03.2022] From a quick test, ethylvanillin seems to have a decent solubility in toluene, so if the solubility data for protocatechuic aldehyde in the section below are true this could be a very good solvent for recrystallisation. In water, ethylvanillin is less soluble than protocatechuic aldehyde. In toluene, the reverse might be true - but I haven't found concrete data to confirm this.

Further notes:
Better TLC separation is obtained by toluene/ethyl acetate/acetic acid v/v/v 8/2/0.2:

Rf (ethylvanillin) = 0.52
Rf (protocatechuic aldehyde) = 0.19

However, the separation using petrol ether works well enough, and petrol ether is cheaper. For spotting the reaction mixture the addition of acetic acid is not required as the solution is already acidic. For the final product AcOH should be included to reduce tailing. Staining with iodine vapor is more sensitive than 254 nm UV. The TLC plates used were 5x10 cm silica gel 60 F254 glass-backed from Merck.

Ethylvanillin has an intense smell, considerably stronger than vanillin. The product doesn't have the same characteristic odor anymore, but it isn't completely odorless either.

Instead of ethyl acetate, it is likely possible to extract with diethyl ether instead, as the patent does.

The solubility of protocatechuic aldehyde varies from source to source, but I found the following:
  • ~ 50 g/L (cold water)[1]
  • ~ 330 g/L (boiling water)[1]
  • 5.0 g/L (0 °C) (water)[2]
  • 11.7 g/L (15 °C) (water)[2]
  • 1 g/mL in boiling alcohol[1]
  • very soluble in ether[1]
  • poorly soluble in boiling toluene[1]
  • nearly insoluble in cold toluene[1]
  • soluble in chloroform[3]


[1] - Beilsteins Handbuch der organischen Chemie, 4th edition, VIII, 1925, p. 246, full text on archive.org
[2] - J. Chem. Eng. Data 2012, 57, 7, 2018–2022, https://doi.org/10.1021/je300323g
[3] - Neues Handwörterbuch der Chemie, Band 5, 1890, p. 862, https://books.google.de/books?id=CqMEAAAAYAAJ
[4] - Purification of laboratory chemicals, 6th edition, 2009, p. 334
[5] - Verfahren zur Herstellung von Isovanillin, DE69507676

The main source/inspiration was German patent DE69507676:

Attachment: DE000069507676T2_all_pages.pdf (737kB)
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[Edited on 18-3-2022 by Diachrynic]




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[*] posted on 17-3-2022 at 19:23


Hi Diachrynic, very nice, well done!!!
So ethylvanilin is more reactive than vanilin. And also easier to obtain from shops (for ice cream production, for baking etc).




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Diachrynic
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[*] posted on 18-3-2022 at 14:50


Thanks Fery!

Quote: Originally posted by Fery  
And also easier to obtain from shops (for ice cream production, for baking etc).
For me, both are fairly easy to get, with ethylvanillin being slightly more expensive than vanillin. But nothing extreme. And the smell is worth it.

I did some more testing regarding the iron(III) complex. It is described in [1] as "green, and with addition of soda first purple, then red."

A spatula tip of protocatechuic aldehyde (left) and one of ethylvanillin (right) were placed in test tubes along with about 2 mL of distilled water. An ultrasonic cleaner was used to speed up the dissolution. Two clear solutions are obtained:
pa_water.jpg - 128kB

Then, a drop of dilute iron(III) chloride solution was added. There is an immediate color change to dark green in the protocatechuic aldehyde solution. The ethylvanillin takes on a very slight blue color. I diluted some of the green solution to show the color better.
pa_fecl3.jpg - 132kB pa_fecl3_dilute.jpg - 136kB

Adding a solution of sodium carbonate to the small test tube causes a color shift towards orange-red:
pa_fecl3_base.jpg - 130kB

Addition of dilute sulfuric acid to the green solution causes the color to fade and only leaves the faintly yellow color characteristic of Fe(III) behind.

I couldn't resist taking some spectra of the dilute solutions (no concentration was measured) in the visible spectrum:
pa1.png - 76kB pa2.png - 78kB pa3.png - 65kB

For protocatechuic aldehyde with iron(III) chloride, peaks are observed around 415 and 655 nm. With the addition of sodium carbonate, a plateau around 425 nm is observed (it's not a true peak, probably due to the very high absorbance below 400 nm).
Ethylvanillin and iron(III) chloride show a peak around 570 nm.

These results, while giving further confirmation of the identity of the product, also reveal that on the TLC plates the protocatechuic aldehyde spot may be visualized with a FeCl3-solution as a spray-stain. It will appear as a dark green spot. Ethylvanillin is not stained.




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[*] posted on 18-3-2022 at 19:47


Nice work! I worked with 3,4-dihydroxybenzaldehyde a lot in my undergrad lab, as it was the starting material for my total synthesis project. I know that sandy, light brown crystalline stuff well. That's what the commercially available stuff looks like- even from Sigma. I would be careful about recrystallizing it. I tried a few times before and everything I did would just make it worse. The stuff really likes to oxidize. I quickly decided it wasn't worth the effort, because the crude stuff worked fine in my reaction and the product I made with it (the di-TBS ether) was more stable and easier to purify.



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[*] posted on 18-3-2022 at 22:49


Very nice work, Diachrynic! I like these "simple", one step organic conversions. Especially if good smelling compounds are involved. :)

I was surprised by Texium's comment. I read in an old article that those aromatic aldehydes that lack OH substituent on the ring are sensitive to oxidation. For example benzaldehyde itself, but veratraldehyde (3,4-dimethoxy-benzaldehyde) too. On the other hand those that have free OH are much more resistant. Vanillin (or ethyl-vanillin) can be kept "forever" in open air with very small change. Here comes Texium's comment on protocathecuic being sensitive too...

Strange. Organic chemistry never ceases to amaze me. :)
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[*] posted on 19-3-2022 at 06:09


It’s actually not the aldehyde that’s the problem in this case. It’s the catechol.



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[*] posted on 19-3-2022 at 09:11


Yeah, resorcin also turns pink in itself by oxidation from air. No aldehyde group involved. :) Thanks for pointing that out.
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[*] posted on 19-3-2022 at 10:42


Just an idea, but couldn't it be purified by vacuum sublimation in high vacuum so any oxidation is prevented?



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[*] posted on 19-3-2022 at 14:23


Quote: Originally posted by Fery  
Just an idea, but couldn't it be purified by vacuum sublimation in high vacuum so any oxidation is prevented?
According to J. Am. Chem. Soc. 1930, 52, 7, 2988–2994, https://doi.org/10.1021/ja01370a064 protocatechuic aldehyde can indeed be sublimated in high vacuum, providing "long white needles". They don't provide a pressure but state that "a high efficiency mercury-vapor-pump" was used.

The same paper also gives some insight into how much toluene should be used for the recrystallization, 500 mL were employed for a bit more than 3.8 g.

On the note of solubility, Eur. J. Org. Chem., 2014: 111-121, https://doi.org/10.1002/ejoc.201301429 mentions that it is "barely soluble in dry DCM".




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[*] posted on 19-3-2022 at 20:51


Quote: Originally posted by Diachrynic  
On the note of solubility, Eur. J. Org. Chem., 2014: 111-121, https://doi.org/10.1002/ejoc.201301429 mentions that it is "barely soluble in dry DCM".
That’s just not true. I ran my silyl protections in DCM and while it was rather slow to dissolve, it fully dissolved at a concentration of 0.25 M, and could probably have been more concentrated than that.



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[*] posted on 27-3-2022 at 13:47


Quote: Originally posted by Diachrynic  

On the note of solubility, Eur. J. Org. Chem., 2014: 111-121, https://doi.org/10.1002/ejoc.201301429 mentions that it is "barely soluble in dry DCM".


I quickly looked at that paper, it doesnt talk about protocatechuic aldehyde (3,4-dihydroxybenzaldehyde) or dihydroxy variants.
I does have a lot of info on 3,4-Dimethoxy-stuff though (and methylenedioxy).
Maybe the DCM solubility was for the methoxy.
I didnt read it very carefully though.
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[*] posted on 28-3-2022 at 11:06


Quote: Originally posted by Texium  
I ran my silyl protections in DCM and while it was rather slow to dissolve, it fully dissolved at a concentration of 0.25 M, and could probably have been more concentrated than that.
Okay, that sounds like it has a fairly high solubility in DCM then. Thanks for the correction!

Quote: Originally posted by Mateo_swe  
I quickly looked at that paper, it doesnt talk about protocatechuic aldehyde (3,4-dihydroxybenzaldehyde) or dihydroxy variants.
It's in the footnotes, number 23 states:
Quote:
Other aldehydes with additional functional groups were also studied: For example, 3,4-dihydroxybenzaldehyde and derivatives thereof, but they were found to be barely soluble in dry CH2Cl2.

Maybe "they" is referring here to the derivatives, but not the parent aldehyde? If so, then I (and Reaxys) was misinterpreting the text.




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[*] posted on 21-5-2022 at 23:35


Apparently this reaction is, in fact, already known in the literature, see JPH10265428A. I didn't know this when I tried the reaction.

Attachment: JPH10265428A.pdf (180kB)
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[*] posted on 24-5-2022 at 06:45


Quote: Originally posted by Diachrynic  
Vanillin is notoriously hard to turn into protocatechuic aldehyde.


Have you tried Aluminum Triiodide in DMSO?
The AlI3 is made in situ from aluminium powder and iodine.
Seems pretty good, only drawback is that much iodine is used and its a bit expensive.

Gram-Scale Synthesis of Protocatechualdehyde (7a)
To a mixture of AlI3 (38.5 mmol, 1.1 eq) prepared in situ from Al powder
(2.205 g) and I2 (14.655 g, 57.74 mmol) in MeCN (250 mL) was
added DMSO (3.009 g, 38.51 mmol, 1.1 equiv). The mixture was
stirred for 0.5 h at 80 °C, before vanillin (6a; 5.326 g, 35 mmol) was
added in portions. After stirring for 18 h at 80 °C, the reaction mixture
was quenched with aq 2 M HCl (50 mL), and extracted with EtOAc
(3 × 100 mL). The organic phases were combined, washed with sat. aq
Na2S2O3 and brine, and dried (anhyd MgSO4). After filtration, the organic
solvents were removed on a rotary evaporator, and the residue
was purified through flash column chromatography (eluent PE/EtOAc
11:9) to give 7a; yield: 4.413 g (91%).

Hmm, rename to xxx.pdf
It change finename of the attachment somehow.

Attachment: phpx5vw5T (463kB)
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[Edited on 2022-5-24 by Mateo_swe]
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