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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962628Generated: October 30, 2026

Chlorotrimethylsilane → Ethyl [(trimethylsilyl)sulfanyl]acetate

https://huagongshe.com/reaction/962628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantEthyl ThioglycolateHCID 12185—
SolventDiethyl EtherHCID 3283—
ProductEthyl [(trimethylsilyl)sulfanyl]acetateHCID 1331049368.1%

Reaction Steps

To a solution of ethyl mercaptoacetate (9.0 mL, 83.2 mmol) in 15 mL of anhydrous ether under nitrogen atmosphere was added trimethylsilyl chloride (12.0 mL, 94.6 mmol) followed by triethyl amine (13.0 mL, 93.3 mmol) slowly. White precipitates were formed upon addition of triethyl amine. The suspension was allowed to stir at room temperature overnight. The white precipitate was removed by filtration. The filtrate was concentrated on a rotavap. The residue oil was distilled at 40° C. (0.5 mm Hg) to give 10.9 g (68%) of ethyl (trimethylsilylthio)acetate as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05760048
Source datasetuspto-grants-1998_06
ORD IDord-f50ae4673ee942fa9aacbe9f8a11eda1
Source noteuspto-grants-1998_06