Basic information Safety Supplier Related

1-METHYL-1-(TRIMETHYLSILYL)ALLENE

Basic information Safety Supplier Related

1-METHYL-1-(TRIMETHYLSILYL)ALLENE Basic information

Product Name:
1-METHYL-1-(TRIMETHYLSILYL)ALLENE
Synonyms:
  • 1-METHYL-1-(TRIMETHYLSILYL)ALLENE
  • 3-(Trimethylsilyl)-1,2-butadiene
  • 3-(Trimethylsilyl)-1,2-butadiene 98%
  • Buta-2,3-Dien-2-Yl(Trimethyl)Silane
  • Silane, trimethyl(1-methyl-1,2-propadien-1-yl)-
CAS:
74542-82-8
MF:
C7H14Si
MW:
126.27
Product Categories:
  • Allenes
  • Building Blocks
  • Organic Building Blocks
  • Building Blocks
  • Chemical Synthesis
  • Organic Building Blocks
Mol File:
74542-82-8.mol
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1-METHYL-1-(TRIMETHYLSILYL)ALLENE Chemical Properties

Boiling point:
111-112 °C(lit.)
Density 
0.759 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.444(lit.)
Flash point:
19 °F
solubility 
sol CH2Cl2, benzene, THF, Et2O, and most organic solvents.
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Safety Information

Hazard Codes 
F
Risk Statements 
11
Safety Statements 
16
RIDADR 
UN 1993 3/PG 2
WGK Germany 
3

MSDS

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1-METHYL-1-(TRIMETHYLSILYL)ALLENE Usage And Synthesis

Physical properties

bp 111 °C; bp 54–56 °C/90 mmHg

Uses

It is widely used as propargylic anion equivalents; three-carbon synthons for [3 + 2] annulations leading to five-membered compounds including cyclopentenes,4 dihydrofurans, pyrrolines, isoxazoles, furans, and azulenes.

Uses

3-(Trimethylsilyl)-1,2-butadiene may be used for the synthesis of γ-(trimethylsilyl)allylborane.

Preparation

1-methyl-1-(trialkylsilyl)allenes can be conveniently prepared by the method of Vermeer. Silylsubstituted propargyl mesylates thus undergo SN2 displacement by the organocopper reagent generated from methylmagnesium chloride, copper(I) bromide, and lithium bromide 1-Methyl-1-(trimethylsilyl)allene is produced in 52% yield from commercially available (trimethylsilyl)propargyl alcohol in this fashion (eq 1). The t-butyldimethylsilyl and triisopropylsilyl analogs are synthesized by the same method in 90% and 58% yield, respectively. Propargyl alcohols bearing these and other trialkylsilyl groups can be prepared by treatment of propargyl alcohol with n-butyllithium and the appropriate trialkylsilyl chloride. Allenylsilanes bearing other C-1 substituents can be prepared in an analogous manner by using the appropriate Grignard reagents.

1-METHYL-1-(TRIMETHYLSILYL)ALLENESupplier

Meryer (Shanghai) Chemical Technology Co., Ltd.
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