참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Chloroform | HCID 6212 | — |
| 반응물 | Methylamine | HCID 6329 | — |
| 반응물 | 2-Thiophenecarboxylic acid, 3-(chlorosulfonyl)-, methyl ester | HCID 2736733 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | methyl 3-(N-methylsulfamoyl)thiophene-2-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04224445 |
|---|
| 출처 데이터셋 | uspto-grants-1980_09 |
|---|
| ORD ID | ord-cfd42209e65a4dbbbd28443a132897ca |
|---|
| 출처 메모 | uspto-grants-1980_09 |
|---|