HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → N-(3-(4-Carbomethoxyphenyl)-1-methylpropyl)-2-hydroxy-2-(3-trifluoromethylphenyl)ethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2-Amino-1-[3-(trifluoromethyl)phenyl]ethan-1-ol | HCID 30514 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(3-Oxobutyl)benzoic acid methyl ester | HCID 10932640 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-(3-(4-Carbomethoxyphenyl)-1-methylpropyl)-2-hydroxy-2-(3-trifluoromethylphenyl)ethanamine | HCID 20493837 | — |
Reaction Steps
A mixture of 4-(4-carbomethoxyphenyl) butan-2-one (3.0 g) and 2-hydroxy-2-(3-trifluoromethylphenyl) ethanamine (3.0 g) in dry benzene (100 ml) was refluxed under Dean and Stark conditions for 2 hours. The solvent was replaced with methanol (100 ml) and sodium borohydride (2.0 g) was added portionwise with ice cooling. The mixture was stirred at ambient temperature for 2 hours, the solvent was evaporated and the residue was partitioned between water (100 ml) and chloroform (100 ml). The organic phase was dried (MgSO4) and evaporated to an oil, which was chromatographed on silica gel 60 in 3% methanol/chloroform. The title compound was obtained as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04396627 |
| Source dataset | uspto-grants-1983_08 |
| ORD ID | ord-c31c22f76520487db83f593564262688 |
| Source note | uspto-grants-1983_08 |