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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934378Generated: November 1, 2026

tert-Butyldimethylsilyl chloride → HCID 18734916, compound

https://huagongshe.com/reaction/1934378

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 11094543HCID 11094543—
SolventDichloromethaneHCID 6344—
SolventDiisopropylethylamineHCID 81531—
ProductHCID 18734916HCID 1873491681.5%

Reaction Steps

tert-butyldimethylsilyl chloride (1.42 g) was added to a mixture of 4(S)-ethynyl-2-azetidinone (0.78 g) in dichloromethane (10 ml) and ethyldiisopropylamine (2.14 ml) at room temperature. The reaction mixture was stirred overnight, then evaporated in vacuo. The residue was purified by column chromatography on silica gel eluting with n-hexane-ethyl acetate (9:1) to give 1-tert-butyldimethylsilyl-4(S)-ethynyl-2-azetidinone (1.4 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384028B1
Source datasetuspto-grants-2002_05
ORD IDord-7bd1c58b8d574e6d95a211a83096307d
Source noteuspto-grants-2002_05