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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951712Generated: November 4, 2026

Sodium methanethiolate → HCID 67197589, compound

https://huagongshe.com/reaction/1951712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
ReactantHCID 18375727HCID 18375727—
SolventMethanolHCID 887—
ProductHCID 67197589HCID 6719758978.9%

Reaction Steps

To a suspension of 1.81 g (25.8 mmol) sodium methanethiolate in 25 ml methanol was added a solution of 1.35 g (4.31 mmol) 2-methanesulfonyloxymethyl-pyrrolidine-1-carboxylic acid benzyl ester in 25 ml methanol. Conversion was monitored by thin layer chromatography. After complete consumption of the starting material the reaction mixture was diluted with ethyl acetate and washed with two portions of water. The organic layer was dried over sodium sulfate. Flash chromatography gave 0.89 g (3.4 mmol, 78%) (S)-2-methylsulfanylmethyl-pyrrolidine-1-carboxylic acid benzyl ester as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404708B2
Source datasetuspto-grants-2013_03
ORD IDord-dbce9fd544034b888fcc240799b246c6
Source noteuspto-grants-2013_03