HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-(Ethoxycarbonyl)-6-nitrobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Nitrophthalic acid | HCID 69043 | — |
| Product | 2-(Ethoxycarbonyl)-6-nitrobenzoic acid | HCID 12018928 | 74% |
Reaction Steps
A solution of 3-nitrophthalic acid (35 g) in ethanol (300 ml) containing conc. sulfuric acid (20 ml) was heated for 24 hours under reflux. The solvent was distilled off, and the residue was poured into ice-water (700 ml), which was extracted with ethyl acetate. The organic layer was washed with water, which was extracted with an aqueous solution of potassium carbonate. The aqueous layer was made acidic with hydrochloric acid, followed by extraction with methylene chloride. The organic layer was washed with water and dried. The solvent was distilled off to give a solid product (29 g, 74%), which was used in the subsequent reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05128356 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-6c0f696732694d07bf881e6f3f1308d7 |
| Source note | uspto-grants-1992_07 |