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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604650Generated: October 30, 2026

3-Bromo-4-oxo-4-phenylbutanoic acid → HCID 19603693, compound

https://huagongshe.com/reaction/1604650

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-4-oxo-4-phenylbutanoic acidHCID 256295—
ReactantHCID 19603751HCID 19603751—
SolventEthyl AcetateHCID 8857—
ProductHCID 19603693HCID 196036936.6%

Reaction Steps

A solution of 4-tert-butyl-2-[5-(thiocarbamoylmethyl)-benzofuran-2-yl]thiazole (740 mg) and 3-bromo-4-oxo-4-phenylbutanoic acid (600 mg) in ethyl acetate (8.0 ml) was heated under reflux for 13.5 hours. After being cooled, the resulting precipitates were collected by filtration and washed with ethyl acetate. The precipitates were dissolved in ethyl acetate, washed with aqueous sodium hydrogen carbonate solution and brine, dried over magnesium sulfate and concentrated under reduced pressure to give a mixture. The mixture was subjected to column chromatography on silica gel and eluted with a mixture of chloroform, methanol and ethyl acetate (20:1:1 to 20:1:2). The fractions containing object compound were combined and concentrated under reduced pressure to give 4-tert-butyl-2-{5-[(5-carboxymethyl-4-phenylthiazol-2-yl)methyl]benzofuran-2-yl}thiazole (72 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994378
Source datasetuspto-grants-1999_11
ORD IDord-3b8956297f6b41178643647f705e2124
Source noteuspto-grants-1999_11