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HRID 28005作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物ChloroformHCID 6212—
反応物MethylamineHCID 6329—
反応物2-Thiophenecarboxylic acid, 3-(chlorosulfonyl)-, methyl esterHCID 2736733—
溶媒WaterHCID 962—
生成物methyl 3-(N-methylsulfamoyl)thiophene-2-carboxylateHCID 12906749—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04224445
出典データセットuspto-grants-1980_09
ORD IDord-cfd42209e65a4dbbbd28443a132897ca
出典メモuspto-grants-1980_09