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- Posts: 56
- Joined: Sun Sep 26, 2004 1:50 pm
- Location: Brazil
I am doing a silylation of a polyacohol in the presence of 1% chloride (NaCl) using BSTFA as TMS donor. I accomplish my reaction in 1/5 of time if I remove the chloride. I think that is because when I use BSTFA my TMS converts to TMSCl that is a known labile tms donnor.
Am I wrong?