HuagongsheHuagongshe Chemistry Print Report · For research reference only
2'-Aminoacetophenone → 2-Amino-alpha-methylbenzenemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2'-Aminoacetophenone | HCID 11086 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Amino-alpha-methylbenzenemethanol | HCID 112058 | 64% |
Reaction Steps
Sodium borohydride (40 g, 1.0 mol) was added portion wise to a stirred solution of o-aminoacetophenone (80 g) in methanol (800 ml) at 0°, allowing the effervescence to subside between each addition. Cooling was removed and the mixture allowed to warm to reflux temperature to complete the reaction. When cool, the solvent was evaporated and the residue partioned between dichloromethane-water. The organic solution was washed successively with water and brine, dried (anhyd. MgSO4), filtered and evaporated to a light yellow oil which crystallized from petroleum spirit (40°-60°) to give white crystals (52 g, 64%), m.p. 50°-52°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05089504 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-e09b0e34a6584703987db3800aaaedf7 |
| Source note | uspto-grants-1992_02 |