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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6958생성일: 2026년 10월 24일

Triethylamine → Methyl 5-sulfamoylthiophene-2-carboxylate

https://huagongshe.com/ko/reaction/6958

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl AcetateHCID 8857—
반응물1,3-Bis(diphenylphosphino)propaneHCID 81219—
반응물5-Bromo-2-thiophenesulfonamideHCID 1241304—
반응물HCID 178418416HCID 178418416—
촉매palladium(II) acetateHCID 167845—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물Methyl 5-sulfamoylthiophene-2-carboxylateHCID 13425727—

반응 조건

온도100 °C

반응 단계

A mixture of 5-bromothiophene-2-sulfonamide (0.50 g, 2.1 mmol), triethyl amine (1 mL), methanol (1 mL), palladium acetate (0.046 g, 2.1 mmol) and 1,3-bis(diphenylphosphino) propane (0.085 g, 2.1 mmol) (addition in that order) in dimethylformamide (5 mL, anhydrous) is saturated with carbon monoxide gas, at room temperature. This reaction mixture is heated to 100° C. and stirred overnight, under a carbon monoxide atmosphere. 10 mL of brine and 10 mL of ethyl acetate are added to the reaction mixture. The organic phase is separated and the aqueous layer is extracted with 10 mL ethyl acetate. The combined organic layers are dried over sodium sulfate, concentrated in vacuo, and then chromatographed on silica (0–1% methyl alcohol in methylene chloride) to give the title compound, as a yellow solid (0.15 g, 34% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084170B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-7b3ef08a6ec846058fe20b3dbccc2c1d
출처 메모uspto-grants-2006_08