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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297163Generated: October 26, 2026

Methanol → 5-Cyanothiophene-2-sulfonamide

https://huagongshe.com/reaction/1297163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantEthyl AcetateHCID 8857—
Reactant5-Bromo-2-thiophenesulfonamideHCID 1241304—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystHCID 178418397HCID 178418397—
SolventDichloromethaneHCID 6344—
Product5-Cyanothiophene-2-sulfonamideHCID 22019526—

Reaction Steps

A mixture of 5-bromothiophene-2-sulfonamide (0.50 g, 2.1 mmol), zinc cyanide (0.25 g, 2.1 mmol), tetrakis(triphenylphosphine)palladium(0) (0.072 g, 0.06 mmol) in dimethylformamide (5 mL, anhydrous) is placed under microwave radiation (under nitrogen atmosphere, 160° C.) for 15 min. Thin layer chromatography (5% methyl alcohol in methylene chloride) demonstrates the reaction is incomplete. Additional tetrakis-(triphenylphosphine)palladium(0) (0.24 g, 0.2 mmol) and dimethylformamide (10 mL) are added to the reaction mixture and placed under microwave radiation (under nitrogen atmosphere at 160° C.) for 37 min. 10 mL of water and 20 mL of ethyl acetate are added to the reaction mixture. The organic phase is separated and the aqueous layer is extracted with 20 mL ethyl acetate. The combined organic layers are dried over sodium sulfate, concentrated in vacuo, and then chromatographed on silica (0-5% methyl alcohol in methylene chloride) to give the title compound, as a white solid (0.22 g, 57% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250430B2
Source datasetuspto-grants-2007_07
ORD IDord-e2fb2948a3f343139a78a9f020dd6ac2
Source noteuspto-grants-2007_07