HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 3-Thiophenecarboxylic acid, 4-(aminosulfonyl)-, methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methyl 4-(chlorosulfonyl)thiophene-3-carboxylate | HCID 12593671 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Thiophenecarboxylic acid, 4-(aminosulfonyl)-, methyl ester | HCID 3042284 | — |
Reaction Steps
39.9 g (0.166 mole) of methyl 4-chlorosulfonylthiophene-3-carboxylate (VIII) is dissolved in 400 ml of absolute chloroform; ammonia is passed in at room temperature until the mixture has an alkaline reaction. After the mixture has been stirred for a further 3 hours (care being taken that the solution remains alkaline) it is extracted with water and the organic phase is dried and evaporated. The crystalline residue can be recrystallized from ethanol; however, for further use, digestion with ether is sufficient.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04028373 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-ea5cf465562c4a609d34e2c35fc2658b |
| Source note | uspto-grants-1977_06 |