Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503926Generated: November 4, 2026

Tetrabutylammonium Fluoride → (S)-3-(4-mercapto-phenyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/503926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant(S)-3-[4-(2-trimethylsilanyl-ethylsulfanyl)-phenyl]-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 59428461—
ReactantKHSO4 Na2SO4HCID 86586342—
Product(S)-3-(4-mercapto-phenyl)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 5942841064%

Reaction Steps

A mixture of (S)-3-[4-(2-trimethylsilanyl-ethylsulfanyl)-phenyl]-pyrrolidine-1-carboxylic acid tert-butyl ester (613 mg, 1.615 mmol) and tetrabutylammoniumfluoride (1.0 M in THF, 10.5 mL) was stirred overnight. A solution of 10% KHSO4/Na2SO4 was then added and the resulting mixture was extracted with EtOAc. The combined organic extracts were washed with brine, dried over Na2SO4, filtered, and evaporated under reduced pressure. The residue was purified via flash chromatography (hexane/EtOAc, 91/9) to give 288 mg (64% yield) of (S)-3-(4-mercapto-phenyl)-pyrrolidine-1-carboxylic acid tert-butyl ester as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776910B2
Source datasetuspto-grants-2010_08
ORD IDord-0af32b28c74c45e1a56c108d593eb33f
Source noteuspto-grants-2010_08