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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590059Generated: November 5, 2026

Sodium borohydride → 3-Mercapto-2,2-dimethyl-1-propylsulfonamide

https://huagongshe.com/reaction/1590059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-Thiocyanato-2,2-dimethyl-1-propanesulfonamideHCID 10443054—
SolventEthanolHCID 702—
Product3-Mercapto-2,2-dimethyl-1-propylsulfonamideHCID 1046498216.8%

Reaction Steps

To a solution of 5.15 g of 3-thiocyanato-2,2-dimethyl-1-propanesulfonamide in 100 ml of ethanol was little by little added 0.79 g of sodium borohydride with stirring and nitrogen gas atmosphere, taking an hour. The reaction mixture was refluxed for an hour and concentrated under reduced pressure. To the residue were added 20 ml of water and 30 ml of 1N-hydrochloric acid. The organic layer was collected, and the aqueous layer was washed with ethyl acetate (50 ml×3). The combined organic layers were dried over anhydrous magnesium sulfate and distilled to remove the solvent. The residue was subjected to a silica gel chromatography, eluting with chloroform-methanol (10:1), to obtain 0.76 g of 3-mercapto-2,2,-dimethyl-1-propanesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05202324
Source datasetuspto-grants-1993_04
ORD IDord-6c1799510e294a22a6c786c5b4acda47
Source noteuspto-grants-1993_04