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Topic: Reaction of aldehyde with PCl5  (Read 16539 times)

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Offline SinkingTako

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Reaction of aldehyde with PCl5
« on: August 18, 2013, 08:21:53 AM »
Hello, I'm confused regarding the reaction of PCl5 with aldehydes. I know that benzaldehyde will react with PCl5 to form benzoyl chloride. Is this reaction specific to benzaldehyde or can this reaction be applied to all C=O groups in general (to form CCl2)?

Also it's stated somewhere that CCl2 groups hydrolyse in H2O to form C=O group. (from some fishy source). Can I clarify if this is correct, and what are the exact conditions involved?

Thank you!
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Offline opsomath

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Re: Reaction of aldehyde with PCl5
« Reply #1 on: August 19, 2013, 09:09:02 AM »
Quote
I know that benzaldehyde will react with PCl5 to form benzoyl chloride

I'm afraid you've gotten benzaldehyde (PhCHO) mixed up with benzoic acid (PhCOOH). PCl5 generally converts ketones and aldehydes from R-CO-R' or R-CO-H to R-CCl2-R' / R-CCl2-H respectively.

In other words, this reagent sucks the oxygen out of carbonyls and replaces with two chlorine atoms instead. :)

Offline insertwittyname

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Re: Reaction of aldehyde with PCl5
« Reply #2 on: October 03, 2014, 01:34:28 PM »
So, if I needed to add only one chlorine atom to a carbonyl group, will I have to reduce the carbonyl to an alcohol before reacting it with PCl5?

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