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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710122Generated: October 31, 2026

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

https://huagongshe.com/reaction/1710122

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]D26° =-52° (dichloromethane); mp 48°-49° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04952600
Source datasetuspto-grants-1990_08
ORD IDord-31a6386a38b241fb8a12829b374cf699
Source noteuspto-grants-1990_08