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Theoretical Synthesis of 3,4,5-Alkoxy-PEA
Why? Because without references all this is nothing but idle speculation. Sergei_Eisenstein and Nico ...
6-5-2005 at 12:57
by: Kinetic
P2P via Tosic acid. Results.
How to make propenylbenzenes from propiophenones? I thought you would know, especially as I linked a ...
25-4-2005 at 13:00
by: Kinetic
Boiling points
Nice work, thanks for sharing.
This should work on the more interesting propenylbenzenes too, which ...
25-4-2005 at 10:46
by: Kinetic
Organic Syntheses
There is a procedure given in OrgSyn for this transformation, but it isn't particularly nice. T ...
20-4-2005 at 10:42
by: Kinetic
Directly related references
The following references should complement garage_chemist's procedure. All the below references ...
29-3-2005 at 13:22
by: Kinetic
Propenylbenzene
Propenylbenzene is pretty stable, and I wouldn't worry about if your only concern is the inert ...
29-3-2005 at 12:53
by: Kinetic
Asarone analogue isomers
Hi FF
Nice to see yet another bee sigining up here.;)

You will get a mixture of isomers, the pre ...
28-3-2005 at 07:12
by: Kinetic
Testing for adulterants
I don't know whether potassium bisulfate is soluble in sulfuric acid or not, so I can't co ...
27-3-2005 at 12:51
by: Kinetic
Removing organic halides
The first idea which came to me was refluxing the acid in concentrated HI, a method that has been kn ...
21-3-2005 at 13:27
by: Kinetic
Oximes to nitroalkanes
When searching for articles on the oxidation of oximes to nitroalkanes yesterday I found a very usef ...
7-3-2005 at 15:06
by: Kinetic
Oxidation states
The prefixes and suffixes correspond to the oxidation state of the element upon which the name of th ...
6-3-2005 at 15:03
by: Kinetic
Article
This is a neat article, although I am a little put off by the use of mercury. I remember this was or ...
5-3-2005 at 15:14
by: Kinetic
Nitrosation references
I'm certain that the general procedure for propiophenone can be applied to other ketones. As th ...
15-2-2005 at 12:19
by: Kinetic
Nitrosation
This is an old but good route whose precedent has been set by quite a large amount of literature in ...
13-2-2005 at 14:43
by: Kinetic
Dibrominations
Once again I've been beaten to the answer of the original question because of my fondness for l ...
11-2-2005 at 11:59
by: Kinetic
Triethylamine
It's quite strange that your triethylamine has decomposed under storage conditions which reacti ...
18-1-2005 at 09:21
by: Kinetic
Toluene to benzaldehyde
A quick search for toluene to benzaldehyde gave me - unsurprisingly - a lot of hits. The extract fro ...
17-1-2005 at 12:00
by: Kinetic
Fun with Nickel
Actually, Ni (V) complexes [i]do[/i] seem to exist.

According to Gmelin, there are some 23 compou ...
16-1-2005 at 04:04
by: Kinetic
Doing it with yeast
Just for clarification, transforming propiophenone to phenyl-1,2-propanedione is an [i]oxidation[/i] ...
2-1-2005 at 08:25
by: Kinetic
Making phenylacetones
Hi Orgy


'Tis my first post here, but anyway...

How about :

1. Bromination of (substit ...
31-12-2004 at 17:57
by: Kinetic

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