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Ethylenediamine diacetic acid
Possibly imidazolidine as a condensation product
http://pubs.acs.org/doi/abs/10.1021/jo01148a003 |
22-8-2013 at 10:08
by: kch |
Ethylenediamine diacetic acid
How did you dehydrate the reaction? |
22-8-2013 at 07:19
by: kch |
Diethyl 1, 3 acetone dicarboxylate disposal/reaction
You could make the acid anhydride, and I think there's a number of syntheses you could do with it |
20-8-2013 at 06:17
by: kch |
butanoic acid from sandmeyer rxn
[rquote=296244&tid=25686&author=turd]I think you misunderstood OPs question.
I think OP's ... |
20-8-2013 at 05:46
by: kch |
Which is the thermodynamically more stable product?
I believe the first product is formed because it is symmetric. Not sure.
[Edited on 8-18-2013 by kc ... |
17-8-2013 at 18:39
by: kch |
Please can any one help me on epichlorohydrin production method
Diamond, you could do that using either hypochlorous acid (HOCl) and sodium hydroxide or you could u ... |
17-8-2013 at 09:59
by: kch |
Please can any one help me on epichlorohydrin production method
[rquote=295949&tid=25676&author=diamond]Thanks bfesser , I only needed epichlorohydrin pro ... |
17-8-2013 at 08:47
by: kch |
butanoic acid from sandmeyer rxn
I would say that since the lactone hydrolyzes to the acid, a little water would be more favorable |
17-8-2013 at 07:18
by: kch |
Please can any one help me on epichlorohydrin production method
[rquote=295894&tid=25676&author=diamond]HOW Epichlorohydrin is manufactured from Bleach and ... |
16-8-2013 at 19:12
by: kch |
Please can any one help me on epichlorohydrin production method
Slightly off-topic, but on Wikipedia epichlorohydrin is said to be prepared with HOCl and NaOH indus ... |
16-8-2013 at 17:51
by: kch |
Ethylenediamine diacetic acid
[rquote=295233&tid=25527&author=papaya]I'm sorry for off topic, but does anyone know a doabl ... |
9-8-2013 at 14:40
by: kch |
Ethylenediamine diacetic acid
Also, your diagram shows acetylaldehyde, not formaldehyde |
8-8-2013 at 12:27
by: kch |
Ethylenediamine diacetic acid
Wouldn't the imine hydrolyze in the second step reverting back to the diamine? Also your final produ ... |
8-8-2013 at 07:38
by: kch |
Ethylenediamine diacetic acid
Found this... might be worth looking into
[quote]<a href="http://www.organic-chemistry.org/abs ... |
7-8-2013 at 16:53
by: kch |
Ethylenediamine diacetic acid
I don't think it is possible using just ethyldiamine and chloroacetic acid. Might be possible throug ... |
7-8-2013 at 15:30
by: kch |
1-butanol dehydrogenation via heated copper
I'm learning here, bear with me 
<!-- bfesser_edit_tag -->[size=-2][<a href="u2u.php?a ... |
5-8-2013 at 17:12
by: kch |
Does this reaction actually occur?
I was referring to the alkene reduction. Sorry for being unclear. I later found this
https://www.er ... |
5-8-2013 at 06:46
by: kch |
Looking for a good programer
I have a good knowledge of programming, and I do have experience with something of this nature. I do ... |
4-8-2013 at 19:34
by: kch |
1-butanol dehydrogenation via heated copper
Depending on how badly you need it, you could try this:
-Oxidize primary alcohol to butanoic acid ... |
4-8-2013 at 18:53
by: kch |
Does this reaction actually occur?
[rquote=294696&tid=25488&author=plante1999]cookery.[/rquote]
Only interested in alkene redu ... |
4-8-2013 at 15:18
by: kch |
Does this reaction actually occur?
I saw this on Rhodium, does the reduction actually occur? I thought it only occurs with hydrogenatio ... |
4-8-2013 at 15:05
by: kch |
Epoxide reduction
It's going to be very difficult to do this for two reasons. First, you have to protect your existing ... |
2-8-2013 at 07:17
by: kch |
syn-Addition with Benzyne
Does benzyne undergo syn-addition? The synthesis I have in mind is the formation of catechol (1, 2- ... |
1-8-2013 at 15:45
by: kch |
Halohydrin reaction?
I believe that in the presence of H2SO4, an elimination reaction will occur in which the OH group le ... |
25-7-2013 at 06:05
by: kch |
Halohydrin reaction?
How do halohydrins react in the presence of sulfuric acid? Does the halogen leave or does the OH lea ... |
24-7-2013 at 18:57
by: kch |
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