ORGLIST: Removing Iodine & Acetyl chloride

From: Enkay (nalini.patel$##$rediffmail.com)
Date: Fri Apr 21 2006 - 10:15:47 EDT

• Next message: chm4sdw$##$leeds.ac.uk: "ORGLIST: Undesired Mannich product"
• Previous message: will jones: "RE: ORGLIST: Polyethylene oxide polymerization"

I done an acetylation reaction of 3-hydroxy benzldehyde very well using acetyl chloride as acetylating agent and iodine as a powerful catalyst in this solvent-free reaction. But after the reaction completion, in work-up, what should I do to remove both these reagents ? I got that Sodium thiosulfate can be used for iodine but also read that it may also react with my aldehyde. Pls suggest something............ nalini

_______________________________________________
ORGLIST - Organic Chemistry Mailing List
Website / Archive / FAQ: http://www.orglist.net
To post a message (TO EVERYBODY) send to everybody$##$orglist.net
To unsubscribe, send to everybody-request$##$orglist.net the message: unsubscribe your_orglist_password your_address

• Next message: chm4sdw$##$leeds.ac.uk: "ORGLIST: Undesired Mannich product"
• Previous message: will jones: "RE: ORGLIST: Polyethylene oxide polymerization"

This archive was generated by hypermail 2.1.4 : Tue Feb 13 2007 - 14:17:01 EST