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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280745Generated: October 31, 2026

Hydrochloric Acid → tert-Butyl 3-sulfanylpyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1280745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium MethoxideHCID 10942334—
Reactanttert-Butyl 3-(acetylthio)pyrrolidine-1-carboxylateHCID 54776232—
SolventMethanolHCID 887—
Producttert-Butyl 3-sulfanylpyrrolidine-1-carboxylateHCID 13324658116.4%

Reaction Steps

To a 0° C. solution of (RS)-3-acetylsulfanyl-pyrrolidine-1-carboxylic acid tert-butyl ester (1.4 g, 5.07 mmol) in MeOH (15 ml) was added dropwise a suspension of sodium methoxide (0.61 g, 11.3 mmol) in MeOH. After 6 hours stirring at room temperature, the reaction mixture was neutralized with 1N HCl and MeOH was partially evaporated. H2O and ethylacetate were added. The aqueous phase was extracted with ethylacetate, the combined organic phases were washed with brine, dried over Na2SO4, filtered and concentrated to provide (RS)-3-mercapto-pyrrolidine-1-carboxylic acid tert-butyl ester (1.2 g, 100%) as a colorless oil, MS: m/e 130.1 (M-OtBu).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451819B2
Source datasetuspto-grants-2002_09
ORD IDord-5de6308f5bba43c58c0b380742c1fe91
Source noteuspto-grants-2002_09