HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 2-(3-hydroxy-4-nitrophenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-(3-Hydroxy-4-nitrophenyl)acetic acid | HCID 23508325 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Product | Ethyl 2-(3-hydroxy-4-nitrophenyl)acetate | HCID 23508320 | — |
Reaction Steps
A solution of 3-hydroxy-4-nitrophenylacetic acid (4.0 g, prepared according to the procedure described by Meyer et al, J. Med. Chem., 1997, 40, pages 1049-1062) in ethanol (approximately 100 ml) was treated with concentrated hydrochloric acid (5-8 drops) was heated at reflux temperature for 3 hours then evaporated. The residue was dissolved in tert-butyl methylether and the solution was washed with saturated aqueous sodium bicarbonate solution, then with water, then dried, and then evaporated to give the title compound (5.0 g) as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562851B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-fcd261dd0d484a43b8ec1e1a484ca566 |
| Source note | uspto-grants-2003_05 |