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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6957생성일: 2026년 10월 23일

Methanol → 5-Cyanothiophene-2-sulfonamide

https://huagongshe.com/ko/reaction/6957

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물WaterHCID 962—
반응물DimethylformamideHCID 6228—
반응물Ethyl AcetateHCID 8857—
반응물5-Bromo-2-thiophenesulfonamideHCID 1241304—
촉매Zinc cyanide (Zn(CN)2)HCID 11186—
촉매HCID 178418397HCID 178418397—
용매DichloromethaneHCID 6344—
생성물5-Cyanothiophene-2-sulfonamideHCID 22019526—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084170B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-c726936bb48143acb2070697d2b01b54
출처 메모uspto-grants-2006_08