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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830168Generated: November 2, 2026

Potassium Hydroxide → 2-benzylsulfanylmethyl-3-(3-cyano-benzylsulfanyl)-N-cyanomethyl-propionamide

https://huagongshe.com/reaction/1830168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantBenzonitrile, 3-(bromomethyl)-HCID 97249—
Reactantthioacetic acid S-[3-benzylsulfanyl-2-(cyanomethyl-carbamoyl)-propyl]esterHCID 86611134—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-benzylsulfanylmethyl-3-(3-cyano-benzylsulfanyl)-N-cyanomethyl-propionamideHCID 22053975104.8%

Reaction Steps

A solution of thioacetic acid S-[3-benzylsulfanyl-2-(cyanomethyl-carbamoyl)propyl] ester (0.105 g) in dimethylformamide (1 mL) and water (0.8 mL) was cooled on ice and treated with 1 N aqueous potassium hydroxide (0.65 mL). 3-Cyanobenzylbromide (0.129 g) in dimethylformamide (0.8 mL) was added. The reaction mixture was allowed to warm to room temperature while stirring overnight. The reaction mixture was then poured into ice water and extracted with ethyl acetate (50 mL) and washed with water and saturated aqueous sodium chloride. The solution was dried over magnesium sulfate and evaporated to give 2-benzylsulfanylmethyl-3-(3-cyano-benzylsulfanyl)-N-cyanomethyl-propionamide (0.135 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064123B1
Source datasetuspto-grants-2006_06
ORD IDord-1219ba2fc5f44b9d83441c0240370ecf
Source noteuspto-grants-2006_06