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ChemicalBook--->CAS DataBase List--->41108-81-0

41108-81-0

41108-81-0 Structure

41108-81-0 Structure
IdentificationBack Directory
[Name]

TERT-BUTYL TRIMETHYLSILYLACETATE
[CAS]

41108-81-0
[Synonyms]

Einecs 255-222-2
t-Butyl Trimethylsilylacetate
TERT-BUTYL TRIMETHYLSILYLACETATE
tert-butyl 2-trimethylsilylacetate
1,1-dimethylethyl trimethylsilylacetate
(Trimethylsilyl)acetic acid 1,1-dimethylethyl ester
Acetic acid, 2-(trimethylsilyl)-, 1,1-dimethylethyl ester
[EINECS(EC#)]

255-222-2
[Molecular Formula]

C9H20O2Si
[MDL Number]

MFCD00042855
[MOL File]

41108-81-0.mol
[Molecular Weight]

188.34
Chemical PropertiesBack Directory
[Boiling point ]

67 °C13 mm Hg(lit.)
[density ]

0.86 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.417
[Fp ]

42 °C
[solubility ]

Chloroform (Soluble), Methanol (Soluble)
[form ]

Oil
[color ]

Colourless
[BRN ]

1930256
Safety DataBack Directory
[Risk Statements ]

10
[Safety Statements ]

23-24/25
[RIDADR ]

UN 3272 3/PG 3
[WGK Germany ]

3
[F ]

10-21
[HazardClass ]

3.2
[PackingGroup ]

III
Hazard InformationBack Directory
[Description]

TERT-BUTYL TRIMETHYLSILYLACETATE is used to prepare lithium enolates which can be alkylated; can be alkenated with aldehydes and ketones; can be acylated; can be reacted with Group 14 halides.
[Physical properties]

air stable, colorless liquid; bp 67°C/13 mmHg; n20 D 1.4184; 1H NMR (CDCl3, 90 MHz) 0.13 (s, 9H), 1.45 (s, 9H), 1.80 (s, 2H); IR 1710 cm?1.
[Uses]

t-Butyl Trimethylsilylacetate is used to prepare lithium enolates which can be alkylated;can be alkenated with aldehydes and ketones;can be acylated;can be reacted with Group 14 halides.
Most applications require initial formation of the enolate (1) (eq 1), which is obtained as a white solid suspended in THF, stable indefinitely at ?78°C.t-Butyl Trimethylsilylacetate
[Preparation]

an advantage of t-butyl trimethylsilylacetate over its methyl and ethyl ester analogs is that it can be prepared by C-silylation of the lithium enolate of t-butyl acetate at ?78°C in THF (85–90% yield). Under the same conditions the enolates of methyl and ethyl acetate give primarily O-silylated products.The reagent has also been prepared by a rapid boron trifluoride etherate catalyzed reaction of trimethylsilylketene with t-butyl alcohol.
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