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1-Methoxy-1-trimethylsilyloxypropene

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1-Methoxy-1-trimethylsilyloxypropene Basic information
Product Name:1-Methoxy-1-trimethylsilyloxypropene
Synonyms:1-(Trimethylsiloxy)-1-methoxy-1-propene;Methylketene methyl(trimethylsilyl)acetal;Trimethyl(1-methoxy-1-propenyloxy)silane;[(1-METHOXY-1-PROPENYL)OXY]TRIMETHYLSILANE;Methoxytrimethylsilyloxypropene;1-METHOXY-1-TRIMETHYLSILYLOXYPROPENE 95+%;1-Methoxy-1-trimethylsilyloxypropene>;Silane, [(1-methoxy-1-propenyl)oxy]trimethyl-
CAS:34880-70-1
MF:C7H16O2Si
MW:160.29
EINECS:202-110-6
Product Categories:Monoalkoxysilanes;Protection & Derivatization Reagents (for Synthesis);Si (Classes of Silicon Compounds);Si-O Compounds;Synthetic Organic Chemistry;Vinylsilanes, Allylsilanes
Mol File:34880-70-1.mol
1-Methoxy-1-trimethylsilyloxypropene Structure
1-Methoxy-1-trimethylsilyloxypropene Chemical Properties
Boiling point 52 °C / 27mmHg
density 0.87
refractive index 1.4130-1.4160
storage temp. 0-10°C
form clear liquid
Specific Gravity0.87
color Colorless to Almost colorless
CAS DataBase Reference34880-70-1
Safety Information
RIDADR 1993
HazardClass 3
PackingGroup III
HS Code 2931900090
MSDS Information
1-Methoxy-1-trimethylsilyloxypropene Usage And Synthesis
Uses1-Methoxy-1-(trimethylsilyloxy)propene is used to reactive nucleophile in Mukaiyama-type aldol reactions with aldehydes, imines, acetals, dialkoxycarbenium ions, and orthoesters; Michael-type additions to α,β-unsaturated carbonyl compounds; substitution reactions with allylic alcohols and esters; acylations; aminations; hydroxylations; and pericyclic reactions; silylating agent.
Preparationsince the first preparation of a ketene trialkylsilyl acetal by Petrov in 1959 by the reaction of triethylsilane and methyl acrylate, several alternative pathways have been explored. Ainsworth and coworkers prepared 1-methoxy-1-(trimethylsilyloxy)propene in 90% yield by deprotonation of methyl propionate with Lithium Diisopropylamide at -78 °C followed by addition of Chlorotrimethylsilane. Reaction of the lithium enolate of methyl acetate with TMS-Cl provides 65% O-silylated and 35% C-silylated products (eq 1). Substitution on the alcohol portion of the ester favors C-silylation while substitution on the α-carbon favors O-silylation. An increase in the steric bulk of the silylating agent (e.g. use of t-Butyldimethylchlorosilane) results in significantly more O-silylation.
1-METHOXY-1-TRIMETHYLSILYLOXYPROPENE synthesis
storage 1-Methoxy-1-(trimethylsilyloxy)propene is easily hydrolyzed and oxidized by exposure to air. Storage is possible in sealed tubes at rt. Use in a fume hood.
1-Methoxy-1-trimethylsilyloxypropene Preparation Products And Raw materials
Preparation Products1-Cyclohexenyloxytrimethylsilane-->1-(Trimethylsiloxy)cyclopentene
Tag:1-Methoxy-1-trimethylsilyloxypropene(34880-70-1) Related Product Information
tert-Butyldimethylsilyl chloride (1E)-1-tert-Butoxy-1-(trimethylsilyloxy)propene 1-(2-Trimethylsiloxyethoxy)-1-trimethylsiloxy-2-methylpropene 3,4-Dihydro-6-[(tert-butyl)dimethyl silyloxy]-2H-pyran Dimethylketene methyl trimethylsilyl acetal 3,4-Dihydro-6-(trimethylsilyloxy)-2H-pyran 1-Methoxy-1-trimethylsilyloxypropene