HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259252Generated: October 29, 2026
Phthalaldehydic acid → 1-oxo-1H-isochromene-3-carboxylic acid
https://huagongshe.com/reaction/259252
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthalaldehydic acid | HCID 8406 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diethyl bromomalonate | HCID 69637 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 1-oxo-1H-isochromene-3-carboxylic acid | HCID 345561 | — |
Reaction Steps
A mixture of 2- carboxybenzaldehyde (20.0g), diethyl bromomalonate (20.0g) and anhydrous potassium carbonate (20.0g) in ethyl methylketone (200ml.) was heated under reflux, with stirring, for 5 hours. The cooled mixture was evaporated to dryness and water (300ml.) added to the residue. After extraction with a mixture of ether-chloroform, the organic extracts were washed with water, dried and evaporated to dryness. The residual solid was heated under reflux with a mixture of concentrated hydrochloric acid (360ml.) -- acetic acid (240ml.) for 2 hours. After cooling, the mixture was poured into iced water (1,200ml.). Filtration gave the product as a white solid, m.p. 241°-2° (lit mp. 239-240°), (Found: C, 62.87; H, 3.39. C10H6O4 requires C, 63.16; H 3.18).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04036964 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-201fefbd76214ed9a17f4d005d953b7a |
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| Source note | uspto-grants-1977_07 |
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