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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252353Generated: October 25, 2026

Sodium Cyanide → 3-Cyano-N-(1,1-dimethylethyl)thiophene-2-sulfonamide

https://huagongshe.com/reaction/1252353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
Reactant2-BromothiopheneHCID 13851—
Reactant3-bromo-N-tert-butylthiophene-2-sulfonamideHCID 14051925—
SolventDimethylformamideHCID 6228—
Product3-Cyano-N-(1,1-dimethylethyl)thiophene-2-sulfonamideHCID 14254939—

Reaction Steps

A mixture of 197.7 g of 3-bromo-N-(1,1-dimethylethyl)thiophene-2-sulfonamide, 195.9 g of cuprous cyanide and 500 mL of dimethylformamide was heated to 150° for two one half hours at which time none of the bromothiophene remained as indicated by thin layer chromatography. The reaction was cooled to room temperature and poured into 1500 mL of 10% aqueous sodium cyanide. The aqueous mixture was extracted with five, 200 mL portions of ethyl ether and the combined extracts were washed with five, 150 mL portions of water followed by one, 200 mL aqueous sodium chloride wash. After drying over magnesium sulfate, filtration and evaporation of the solvent 140.8 g of the desired product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04743290
Source datasetuspto-grants-1988_05
ORD IDord-a7a24be5e732421085ec0e9f866fe27b
Source noteuspto-grants-1988_05