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Topic: Phenethyl Bromide Synthesis  (Read 11354 times)

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Offline lutesium

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Phenethyl Bromide Synthesis
« on: January 04, 2008, 07:59:39 AM »
How can Phenethyl Bromide synthesised??? Would a deamination of Phenethyl Amine to Phenethyl Alcohol work??? Or is there an easier way???

If we try to halogenate Benzyl Alcohol or Phenethyl Alcohol with a HX which would be easier???


Lutesium....

Offline agrobert

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Re: Phenethyl Bromide Synthesis
« Reply #1 on: January 04, 2008, 01:02:21 PM »
Tosylate the alcohol and then displace it with HBr.
In the realm of scientific observation, luck is only granted to those who are prepared. -Louis Pasteur

Offline Kryolith

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Re: Phenethyl Bromide Synthesis
« Reply #2 on: January 04, 2008, 04:07:22 PM »
If we try to halogenate Benzyl Alcohol or Phenethyl Alcohol with a HX which would be easier???

1. Formation of a resonance stabilized benzyl cation (SN1)-->Addition of halogenide
2. Primary carbon atom --> SN2 reaction, E2 elimination possible

A better way (in both cases) would be the use of SOCl2, PCl3, PCl5 etc. for chlorination or PBr3 (P+Br2) for bromination.


Offline agrobert

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Re: Phenethyl Bromide Synthesis
« Reply #3 on: January 04, 2008, 04:27:53 PM »


1. Formation of a resonance stabilized benzyl cation (SN1)-->Addition of halogenide
2. Primary carbon atom --> SN2 reaction, E2 elimination possible

A better way (in both cases) would be the use of SOCl2, PCl3, PCl5 etc. for chlorination or PBr3 (P+Br2) for bromination.



Right, I wasn't thinking about elimination.  ;)
In the realm of scientific observation, luck is only granted to those who are prepared. -Louis Pasteur

Offline lutesium

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Re: Phenethyl Bromide Synthesis
« Reply #4 on: January 04, 2008, 07:13:00 PM »
So how can phenethyl alcohol be synthesised???


Lutesium...

Offline Kryolith

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Re: Phenethyl Bromide Synthesis
« Reply #5 on: January 05, 2008, 05:20:01 AM »
So how can phenethyl alcohol be synthesised???
There are several ways, for example Friedel-Crafts reaction of benzene and ethylene oxide, Grignard reaction of PhMgBr with ethylene oxide, hydrogenation of styrene oxide with Raney-Ni, reaction of esters of phenylacetetic acid with Na in EtOH etc.

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