HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 3-benzylamino-5-methylsulphamyl-4-phenoxy-benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 3-Amino-5-methylsulphamyl-4-phenoxy-benzoic acid | HCID 21506014 | — |
| Product | Ethyl 3-benzylamino-5-methylsulphamyl-4-phenoxy-benzoate | HCID 21506047 | — |
Reaction Steps
A mixture of 3-amino-5-methylsulphamyl-4-phenoxy-benzoic acid (1 g), benzyl bromide (1.25 g), and dry ethanol (15 ml) was refluxed for 9 hours. After 3 hours and after 6 hours more benzyl bromide (0.6 g) was added. After cooling, the precipitated ethyl 3-benzylamino -5-methylsulphamyl-4-phenoxy-benzoate was collected by suction, recrystallized from ethanol, and dried in vacuo. The melting point of the compound was 162.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03985777 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-19b5246125b84b9faaadb6dce9c3cb41 |
| Source note | uspto-grants-1976_10 |