HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Nitroacetophenone → 1-(3-Aminophenyl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Nitroacetophenone | HCID 8494 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(3-Aminophenyl)ethanol | HCID 222461 | 97% |
Reaction Steps
Following the procedure of Example I there was charged m-nitroacetophenone (33.0 g. 0.20 mole, 99% purity), water (300 ml.), and Raney nickel (14.8 g. (wet), Grace No. 4200) under 300 psi to 250 psi hydrogen. After 21/2 hours, work-up, by complete evaporation of the filtered hydrogenate, yielded 26.7 g. (97% yield) of m-amino-α-methylbenzyl alcohol which was 99.3% pure by GLC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04024187 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-528561af91c94c3fbe6fff1bd94513ce |
| Source note | uspto-grants-1977_05 |