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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265172Generated: October 31, 2026

6-fluoro-4-oxo-4H-chromene-2-carboxylic acid → 6-Fluoro-3,4-dihydro-2H-1-benzopyran-2-carboxylic acid

https://huagongshe.com/reaction/1265172

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-fluoro-4-oxo-4H-chromene-2-carboxylic acidHCID 4096046—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
Product6-Fluoro-3,4-dihydro-2H-1-benzopyran-2-carboxylic acidHCID 1538284383%

Reaction Steps

A mixture of 63.4 parts of 6-fluoro-4-oxo-4H-1-benzopyran-2-carboxylic acid and 400 parts of acetic acid was hydrogenated at normal pressure and at room temperature with 3 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was stirred in petroleumether. The product was filtered off and dried in vacuo at 70° C., yielding 49 parts (83%) of 6-fluoro-3,4-dihydro-2H-1-benzopyran-2-carboxylic acid (int. 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06545040B1
Source datasetuspto-grants-2003_04
ORD IDord-ad9707ec2bf94e2b801764bc2cc1c110
Source noteuspto-grants-2003_04