HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Nitroacetophenone → alpha-Methyl-3-nitrobenzenemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Nitroacetophenone | HCID 8494 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | alpha-Methyl-3-nitrobenzenemethanol | HCID 223135 | 90% |
Reaction Steps
A solution of sodium borohydride (0.4 g, 10 mmol) in ethanol (10 ml) was treated with m-nitroacetophenone (3.3 g, 20 mmol) at 20° C. for 20 mins. The solution was the diluted with aqueous potassium carbonate and extracted with chloroform. The extracts were dried (magnesium sulphate) and evaporated in vacuo to give 1-(m-nitrophenyl)ethanol as an oil (2.9 g, 90%);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04436751 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-64a0de1e16644c6c8d164d9090634157 |
| Source note | uspto-grants-1984_03 |