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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromo-4-oxo-4-phenylbutanoic acid | HCID 256295 | — |
| Reactant | HCID 19603751 | HCID 19603751 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19603693 | HCID 19603693 | 6.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05994378 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-3b8956297f6b41178643647f705e2124 |
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| Source note | uspto-grants-1999_11 |
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