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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chloroform | HCID 6212 | — |
| Edukt | Methylamine | HCID 6329 | — |
| Edukt | 2-Thiophenecarboxylic acid, 3-(chlorosulfonyl)-, methyl ester | HCID 2736733 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | methyl 3-(N-methylsulfamoyl)thiophene-2-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04224445 |
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| Quelldatensatz | uspto-grants-1980_09 |
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| ORD ID | ord-cfd42209e65a4dbbbd28443a132897ca |
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| Quellennotiz | uspto-grants-1980_09 |
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