| Identification | Back 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 Properties | Back 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 | [InChI]
1S/C9H20O2Si/c1-9(2,3)11-8(10)7-12(4,5)6/h7H2,1-6H3 | [InChIKey]
HOHBQWITMXOSOW-UHFFFAOYSA-N | [SMILES]
CC(C)(C)OC(=O)C[Si](C)(C)C |
| Safety Data | Back 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 | [Storage Class]
3 - Flammable liquids | [Hazard Classifications]
Flam. Liq. 3 |
| Hazard Information | Back 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. | [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. |
|
| Company Name: |
Sigma-Aldrich
|
| Tel: |
021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
| Company Name: |
Alfa Chemistry
|
| Tel: |
1-516-6625404 |
| Website: |
https://www.alfa-chemistry.com |
|