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Merck
CN

209120

Sigma-Aldrich

(三甲基硅基)乙酸乙酯

≥98%

别名:

ETSA

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About This Item

线性分子式:
(CH3)3SiCH2CO2C2H5
CAS号:
分子量:
160.29
Beilstein:
1755902
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

≥98%

表单

liquid

折射率

n20/D 1.415 (lit.)

沸点

156-159 °C (lit.)

密度

0.876 g/mL at 25 °C (lit.)

SMILES字符串

CCOC(=O)C[Si](C)(C)C

InChI

1S/C7H16O2Si/c1-5-9-7(8)6-10(2,3)4/h5-6H2,1-4H3

InChI key

QQFBQBDINHJDMN-UHFFFAOYSA-N

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一般描述

Reaction of ethyl trimethylsilylacetate (ETSA) with dilute hydrochloric acid, dilute alkali, anhydrous HCl, anhydrous bromine and absolute ethanol has been reported. ETSA undergoes condensation with aromatic aldehydes in the presence of base catalyst to yield β-trimethylsiloxycarboxylates. Lithium ETSA reacts with ketones to yield α,β-unsaturated esters.

应用

Ethyl trimethylsilylacetate (ETSA) was used in the synthesis of ethyl-2,2-dibromo-2-(trimethylsilyl)acetate. It was also used to silylate the enolizable aldehydes and ketones

象形图

Flame

警示用语:

Danger

危险声明

危险分类

Flam. Liq. 2

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

<73.4 °F - closed cup

闪点(°C)

< 23 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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分析证书(COA)

Lot/Batch Number

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Synthetic Communications, 19, 2441-2441 (1989)
New synthesis of. alpha.,. beta.-unsaturated carboxylic esters.
Shimoji K, et al.
Journal of the American Chemical Society, 96(5), 1620-1621 (1974)
Synthesis and Cleavage of Ethyl Trimethylsilylacetate1, 2.
Gold JR, et al.
Journal of the American Chemical Society, 70(9), 2874-2876 (1948)
Journal of the Chemical Society. Perkin Transactions 1, 3217-3217 (1988)
Mitsuru Shindo et al.
Chemical & pharmaceutical bulletin, 51(4), 477-478 (2003-04-04)
Aliphatic alpha,alpha-dibromo esters, precursors of ynolates, were synthesized via bromination of lithium alpha-bromo ester enolates with 1,2-dibromotetrafluoroethane in good yields. alpha-Trimethylsilyl-alpha,alpha-dibromo esters were synthesized via radical bromination.

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