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Topic: Protection of Benzyl alcohol  (Read 6247 times)

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Offline GSR

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Protection of Benzyl alcohol
« on: February 09, 2006, 10:30:29 AM »
Hi,

I am trying to protect the -OH group of a substituted benzyl alcohol with p-toulenesulfonyl chloride but it seems the reaction did not worked well. can anybody suggest ways( economical with good yield)  to protect/deprotect the -OH group of these kind of benzyl alcohol derivatives.

thanks in advance.

GSR

forislam20

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Re:Protection of Benzyl alcohol
« Reply #1 on: February 09, 2006, 11:14:51 AM »
TRY RPOTECTION WITH CH3I AND NaOH AND DEPROTECTION USING HI

Offline GSR

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Re:Protection of Benzyl alcohol
« Reply #2 on: February 09, 2006, 11:32:02 AM »
can you be more specific  with details and references??

Offline movies

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Re:Protection of Benzyl alcohol
« Reply #3 on: February 09, 2006, 02:48:52 PM »
A methyl ether can be a very difficult protecting group to cleave.

Are you set on using a Ts group?  What about a silyl ether like trimethylsilyl (TMS)?

What are you protecting from?  What other functional groups are in your molecule?  How would they be affected by protection/deprotection methods?

There are lots of things to consider when it comes to PGs!!

Offline plu

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Re:Protection of Benzyl alcohol
« Reply #4 on: February 10, 2006, 11:21:55 AM »
Another alternative: dihydropyran

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