HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-Hydroxy-3-nitrophenyl)-ethanone → 3-Amino-2-hydroxyacetophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-Hydroxy-3-nitrophenyl)-ethanone | HCID 270026 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Amino-2-hydroxyacetophenone | HCID 459294 | — |
Reaction Steps
A solution of 2-hydroxy-3-nitroacetophenone [4.0 g; prepared by the method of Allen et al., J. Chem. Soc., (1949), 821] in ethanol (150 ml) was hydrogenated at 25° C. and 50 p.s.i. for 2.5 hours, using a catalyst of platinum on charcoal. The mixture was filtered and the filtrate was evaporated in vacuo to give a black solid, which was purified by chromatography on a column of silica gel, using diethyl ether as eluant. The fastest moving band (yellow) was collected to give 3-amino-2-hydroxyacetophenone (3.0 g), in the form of a bright yellow solid, m.p. 95°-97° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04442115 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-6e1246759c8e40a4a9620a08b5184f21 |
| Source note | uspto-grants-1984_04 |