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General and efficient method for the synthesis of alkoxymethylsilanes
Author(s) -
Suga Seiji,
Miyamoto Keiko,
Watanabe Mitsuru,
Yoshida Junichi
Publication year - 1999
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/(sici)1099-0739(199906)13:6<469::aid-aoc872>3.0.co;2-a
Subject(s) - chemistry , steric effects , halogenation , triethylamine , alkoxide , azobisisobutyronitrile , cationic polymerization , borane , hydride , substitution reaction , alkoxy group , substitution (logic) , organic chemistry , medicinal chemistry , catalysis , monomer , alkyl , hydrogen , polymer , computer science , programming language
Although alkoxymethylsilanes serve as useful building blocks, various efforts to synthesize them by substitution reaction with an alkoxide ion at the carbon adjacent to the silicon failed. To solve this synthetic problem a new route which is very simple to perform was developed. Bromination of (methoxymethyl)trimethylsilane by using N ‐bromosuccinimide/2,2′‐azobisisobutyronitrile (NBS/AIBN) was followed by a substitution by alcohols in the presence of triethylamine to give the corresponding [alkoxy‐(methoxy)methyl]trimethylsilanes. These acetals can be used directly for the next reduction with di‐isobutylaluminium hydride (DIBAL‐H) or Et 3 SiH/BF 3 ·OEt 2 to give alkoxymethylsilanes in good to moderate yields. The success of the substitution reaction with the alcohols suggests that the mechanism is of somewhat S N 1 by nature and formation of the cationic intermediate seems to release the steric hindrance around the carbon, allowing the attack of alcohols. Copyright © 1999 John Wiley & Sons, Ltd.