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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107971Generated: October 28, 2026

Triethylamine → (S)-3-((tert-Butyldimethylsilyl)oxy)pyrrolidin-2-one

https://huagongshe.com/reaction/2107971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(3S)-3-hydroxypyrrolidin-2-oneHCID 11029774—
SolventDichloromethaneHCID 6344—
Product(S)-3-((tert-Butyldimethylsilyl)oxy)pyrrolidin-2-oneHCID 1058480472.1%

Reaction Steps

A mixture of 14 g of (S)-3-hydroxy-2-pyrrolidinone, 45 g of tert-butyldimethylsilyl chloride, 50 ml of triethylamine and 500 ml of dichloromethane was stirred overnight. The solution was washed four times with water, once with brine, dried and concentrated in vacuo. The residue was dissolved in 500 ml of methanol, refluxed overnight and concentrated in vacuo. The residue was purified by chromatography (silica gel), giving 21.5 g of (S)-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-pyrrolidinone; [α]D260 =-52° (dichloromethane); mp 48°-49° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04937235
Source datasetuspto-grants-1990_06
ORD IDord-73f887c7df9741d5bf6c52c2c493b25b
Source noteuspto-grants-1990_06