HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4-(4-Methylphenyl)-3-phenylbutan-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 4-(4-Methylphenyl)-3-phenylbutan-2-one | HCID 12615793 | — |
| Solvent | Ammonia | HCID 222 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(4-Methylphenyl)-3-phenylbutan-2-amine | HCID 22270653 | — |
Reaction Steps
To a solution of the 4-(4-methylphenyl)-3-phenylbutan-2-one (308 mg, 1.29 mmol) in 7M ammonia in MeOH (5 mL) and acetic acid (3 mL) was added sodium cyanoborohydride (130 mg, 2.06 mmol) and the reaction stirred at room temperature overnight. The reaction was quenched by pouring into 2M sodium carbonate solution and extracted into EtOAc. The aqueous layer was salted and re-extracted. The combined organic extracts were dried over MgSO4 and concentrated to give the title compound as a mixture of 4 isomers which was used without further purification. LC-MS: m/e 240 (M+H)+ (2.22 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07423067B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-e81f9d9a062a471d8be0ce9ae7bf2ee2 |
| Source note | uspto-grants-2008_09 |