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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704109Generated: October 31, 2026

Hydrochloric Acid → 6-fluoro-4-oxo-3,4-dihydro-2H-1-benzopyran-2-carboxylic acid

https://huagongshe.com/reaction/704109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(5-Fluoro-2-hydroxyphenyl)-4-oxobut-2-enoic acidHCID 14555258—
SolventWaterHCID 962—
Product6-fluoro-4-oxo-3,4-dihydro-2H-1-benzopyran-2-carboxylic acidHCID 2778525—

Reaction Steps

Sodium bicarbonate (2.10 g, 25.0 mmol) was added to a suspension of (E)-4-(5-fluoro-2-hydroxyphenyl)-4-oxo-2-butenoic acid (5.00 g, 23.8 mmol) (obtained through the process as described in Example 22) in 200 ml of distilled water and the mixture was refluxed for 10 minutes. After cooling, the reaction mixture was acidified to pH 1.0 with concentrated hydrochloric acid and then extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and evaporated in vacuo to give crude crystals which were recrystallized from the mixture of water and methanol to give 4.60 g (92.1%) of the subject desired compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985574
Source datasetuspto-grants-1991_01
ORD IDord-883b91a1c0324a7f9ff766ba3297ff6b
Source noteuspto-grants-1991_01