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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467078Generated: October 25, 2026

Trifluoroacetic acid → 5-Bromochroman-3-one

https://huagongshe.com/reaction/467078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-Ethoxycarbonyl-5-bromo-3-chromanoneHCID 19043193—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product5-Bromochroman-3-oneHCID 1904318653%

Reaction Steps

A suspension of 2-ethoxycarbonyl-5-bromo-3-chromanone (300 mg, 1 mMol) in methanol (5 mL) and 10% hydrochloric acid (3 mL) was heated at reflux for 2 hours. All of the solid had not dissolved; therefore, trifluoroacetic acid (1 mL) was added, and heating was continued for 18 hours. The reaction mixture was diluted with water and extracted well with diethyl ether. The ether phases were combined, dried over sodium sulfate, and concentrated in vacuo to give a yellow glass. Purification by flash chromatography (1:1 hexane:ether) gave the title compound as a light yellow glass (120 mg, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05158956
Source datasetuspto-grants-1992_10
ORD IDord-42843c29f04f404abe748547c37686fa
Source noteuspto-grants-1992_10