HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 3-benzylamino-5-sulphamyl-4-(beta,beta, beta-trifluoroethoxy)-benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 3-Amino-5-sulphamyl-4-(beta,beta,beta-trifluoroethoxy)-benzoic acid | HCID 21506001 | — |
| Product | Ethyl 3-benzylamino-5-sulphamyl-4-(beta,beta, beta-trifluoroethoxy)-benzoate | HCID 21505983 | — |
Reaction Steps
A mixture of 3-amino-5-sulphamyl-4-(β, β, β-trifluoroethoxy)-benzoic acid (0.6 g), benzyl bromide (1.2 g), and dry ethanol (8 ml) was refluxed for 5 hours. After cooling, the precipitated ethyl 3-benzylamino-5-sulphamyl-4-(β, β, β-trifluoroethoxy)-benzoate was collected by suction and recrystallized from dry ethanol. After drying, the compound had a melting point of 163-165°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03971819 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-a62ca07907e445099d9446cee06bad31 |
| Source note | uspto-grants-1976_07 |