HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 3-hydroxy-5-nitro-4-phenylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Hydroxy-5-nitro-4-phenylbenzoic acid | HCID 21546850 | — |
| Product | Ethyl 3-hydroxy-5-nitro-4-phenylbenzoate | HCID 21546856 | — |
Reaction Steps
A mixture of 3-hydroxy-5-nitro-4-phenylbenzoic acid (22 g; prepared as in Example 2, step B), conc. sulfuric acid (10 ml) and ethanol (400 ml) is refluxed for 20 hours. The resulting solution is concentrated in vacuo to about 100 ml and is then diluted with water (about 300 ml). The separated ethyl 3-hydroxy-5-nitro-4-phenylbenzoate is collected by filtration, washed with water and dried. After recrystallization from carbon tetrachloride, the ester is obtained with a melting point of 128°-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03950380 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-5bb7d02f634e487197aeaecae7bac572 |
| Source note | uspto-grants-1976_04 |