January 11, 2025, 07:48:44 AM
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Topic: heterocyclic chemistry  (Read 1882 times)

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Offline debabrata

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heterocyclic chemistry
« on: December 23, 2014, 12:59:11 AM »
what happens when x's bromine reacts with benzothiophene in chloroform at r.t. I think initially it should add to 3- position ( sigma-complex more stable for 3-position than 2- position ) .I think the 2nd eqv. should add to 5- position , but I'm not sure.

Offline billnotgatez

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Re: heterocyclic chemistry
« Reply #1 on: December 23, 2014, 06:49:13 AM »
x's 
r.t.
eqv.

Sigh

Offline OrgXemProf

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Re: heterocyclic chemistry
« Reply #2 on: December 25, 2014, 07:52:14 PM »
Seems perfectly clear, imho.

x's = excess
r. t. = room temperature
eqv. = equivalents


Check Section 21.1.1 in John A. Joule & Keith Mills, "Heterocyclic Chemistry", 5th Edition, 2010, Wiley:New York to see what they have to say about reacting benzothiophene with Br2 and their suggestion concerning a better way to prepare 3-benzothiophene.

Then, you might check their suggestion regarding the structure of the corresponding dibromobenzothiophene.



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