HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 4-Methyl-1-oxo-1H-2-benzopyran-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Acetylbenzoic acid | HCID 68474 | — |
| Reactant | Diethyl bromomalonate | HCID 69637 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Methyl-1-oxo-1H-2-benzopyran-3-carboxylic acid | HCID 12388295 | — |
Reaction Steps
A mixture of 2- acetylbenzoic acid (6.21g), diethyl bromomalonate (9.0g.) and potassium hydroxide (2.12g.) in ethanol (50ml.) was heated under reflux for 6 hours. The cooled mixture was evaporated to dryness, water (100ml.) added and extracted with ether. The combined ethereal extracts were washed with water, dried and evaporated to dryness. The residue was heated under reflux with a mixture of concentrated hydrochloric acid (160ml.) -- acetic acid (100ml.) for two hours, cooled poured into iced water (1 liter). Filtration gave the product as a white solid, mp. 250° -2°, (lit mp. 248° -9°) (Found: C, 64.59; H, 4.01. C11H8O4 requires C, 64.70; H, 3.95).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04036964 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-1a9e4bed730a48dfb4c25b62fccca76d |
| Source note | uspto-grants-1977_07 |