Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111186Generated: October 29, 2026

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

https://huagongshe.com/reaction/1111186

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 numberUS04978758
Source datasetuspto-grants-1990_12
ORD IDord-721c77d1541143ffbe1b6431764c7e05
Source noteuspto-grants-1990_12