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Topic: how can i find the synthesis scheme as well as reaction conditions (benzylamine)  (Read 4127 times)

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Offline Stundt

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Hi,

i want to synthesise Benzylamine  ?
so i have gone thru the preparations in the general org. text books but i need the procedure for doing the experiment
I hav evem gone thru Vogel's Practical Org .Chem


how can i get all the possible ways of synthesise benzylamine:
AS BENZYLAMINE WILL BE THE REAGENT FOR BY PROJECT

Regards
Stnd
                    HAVE A NICE DAY!

Offline discodermolide

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Hi,

i want to synthesise Benzylamine  ?
so i have gone thru the preparations in the general org. text books but i need the procedure for doing the experiment
I hav evem gone thru Vogel's Practical Org .Chem


how can i get all the possible ways of synthesise benzylamine:
AS BENZYLAMINE WILL BE THE REAGENT FOR BY PROJECT

Regards
Stnd
                    HAVE A NICE DAY!





By benzyl chloride, do a nucleophillic displacement of the chloride with azide. Then hydrogenolyse the benzyl azide.

« Last Edit: March 27, 2012, 04:33:44 PM by Borek »
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Offline cakaro13

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Starting from benzene, you could do FC acylation, then reductive amination. The previous synthesis sounds a bit simpler though.

Offline discodermolide

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Starting from benzene, you could do FC acylation, then reductive amination. The previous synthesis sounds a bit simpler though.

A Friedel-Crafts acylation, with what?
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Offline pacifyer

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Try a Gabriel synthesis...  ;)

Offline Honclbrif

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Dude, just buy it. Its cheaper than pretty much any reasonable starting material.
Individual results may vary

Offline Stundt

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hmmmmmmm

I prefer buying the reagent
Actually running out of time so i prefer buying thanks  Honclbrif for the advice

I would hav prepared from benzyl chloride but therez a problem with that it forms byproducts like dibenzyl chloride and tertiary products




Thanks for the replies
                         

Offline discodermolide

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hmmmmmmm

I prefer buying the reagent
Actually running out of time so i prefer buying thanks  Honclbrif for the advice

I would hav prepared from benzyl chloride but therez a problem with that it forms byproducts like dibenzyl chloride and tertiary products




Thanks for the replies
                         



No it doesn't, you get a very clean product with this azide reaction. I've done it many times on very large scale.
Development Chemists do it on Scale, Research Chemists just do it!
My Research History

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