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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 28005Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroformHCID 6212—
EduktMethylamineHCID 6329—
Edukt2-Thiophenecarboxylic acid, 3-(chlorosulfonyl)-, methyl esterHCID 2736733—
LösungsmittelWaterHCID 962—
Produktmethyl 3-(N-methylsulfamoyl)thiophene-2-carboxylateHCID 12906749—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04224445
Quelldatensatzuspto-grants-1980_09
ORD IDord-cfd42209e65a4dbbbd28443a132897ca
Quellennotizuspto-grants-1980_09