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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233952Generated: October 25, 2026

Trifluoroacetic acid → 2-Carboxymethyl-3-(ethoxycarbonylmethoxy)bromobenzene

https://huagongshe.com/reaction/233952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-Ethoxycarbonyl-5-bromo-3-chromanoneHCID 19043193—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-Carboxymethyl-3-(ethoxycarbonylmethoxy)bromobenzeneHCID 1904320953%

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 numberUS05594034
Source datasetuspto-grants-1997_01
ORD IDord-39c4d85ee08a4e5096c2f0671a447ac5
Source noteuspto-grants-1997_01