HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 1-(4'-Amino-3'-trifluoromethyl-phenyl)-2-tert.pentylamino-ethanol hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 1-(4'-Amino-3'-bromo-5'-trifluoromethyl-phenyl)-2-tert.pentylamino-ethanol hydrochloride | HCID 13355640 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(4'-Amino-3'-trifluoromethyl-phenyl)-2-tert.pentylamino-ethanol hydrobromide | HCID 13355763 | — |
Reaction Steps
5 gm of 1-(4'-amino-3'-bromo-5'-trifluoromethyl-phenyl)-2-tert.pentylamino-ethanol hydrochloride were distributed between ethyl acetate and 2N ammonia. The organic layer was dried and evaporated in vacuo, the residual base was dissolved in 100 ml of methanol in a hydrogenation vessel. 2.5 gm of palladium oxide/barium sulfate catalyst (5%) were added, and the mixture was hydrogenated until 1 mol of hydrogen had been absorbed. After the catalyst had been removed by filtration, the filtrate was evaporated in vacuo, and the solid residue was recrystallized from isopropanol. The obtained hydrobromide melted at 174°-175° C. (decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04119710 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-630efa2be383451c87d948a961490177 |
| Source note | uspto-grants-1978_10 |