HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 4-(4-Methoxybenzoyl)thiophene-2-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(4-Methoxybenzoyl)thiophene-2-sulfonic acid | HCID 14639067 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Methoxybenzoyl)thiophene-2-sulfonamide | HCID 14639069 | — |
Reaction Steps
To 2.98 g (0.01 mol) of product from Step B suspended in 75 ml CH2Cl2 was added excess thionyl chloride and the resulting suspension was stirred, and heated at reflux for 1.5 hours to give a homogeneous solution. The thionyl chloride was evaporated and the residue was extracted with CHCl3 after ice had been added. The organic extract was washed with brine, dried and the solvent evaporated to give a yellow oil. This was taken up in acetone and treated with 5 ml of concentrated NH4OH dropwise. After stirring for 15 minutes, this was extracted with chloroform and the extract was dried. Filtration and evaporation of the solvent gave the desired product as a yellow solid, m.p. 173°-175° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04914111 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-2ac3e362dc4d42f38ee2385855534612 |
| Source note | uspto-grants-1990_04 |