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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28005생성일: 2026년 10월 23일

Chloroform → methyl 3-(N-methylsulfamoyl)thiophene-2-carboxylate

https://huagongshe.com/ko/reaction/28005

반응식

참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물MethylamineHCID 6329—
반응물2-Thiophenecarboxylic acid, 3-(chlorosulfonyl)-, methyl esterHCID 2736733—
용매WaterHCID 962—
생성물methyl 3-(N-methylsulfamoyl)thiophene-2-carboxylateHCID 12906749—

반응 단계

43.5 G. (0.18 mol) of the obtained 3-chlorosulfonylthiophene-2-carboxylic acid methyl ester are dissolved in 450 ml. of absolute chloroform and dry methylamine is led through the solution at 10° C. until a moistened pH paper shows an alkaline reaction with the solution. The mixture is then allowed to react at room temperature for a further 2 hours, the solution always remaining alkaline. The solution is then shaken out with 500 ml. of water and 500 ml. of a 5% sodium bicarbonate solution [the aqueous phases are back-extracted in each case once with chloroform]. The combined organic phases are dried over sodium sulfate and then evaporated. The crystalline residue is digested with ether for purification. There is obtained 3-methylsulfamoylthiophene-2-carboxylic acid methyl ester of melting point 115°-122° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04224445
출처 데이터셋uspto-grants-1980_09
ORD IDord-cfd42209e65a4dbbbd28443a132897ca
출처 메모uspto-grants-1980_09