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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534233Generated: November 2, 2026

HCID 14579738, compound → HCID 14579736, compound

https://huagongshe.com/reaction/1534233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14579738HCID 14579738—
CatalystCopperHCID 23978—
SolventQuinolineHCID 7047—
ProductHCID 14579736HCID 1457973675%

Reaction Steps

A mixture of 3-methyl-4-hydroxy-5-propyl-7-fluorobenzofurancarboxylic acid (0.10 gm; 0.4 mmoles) and copper(20 mg) in quinoline (50 mL) was refluxed for a period of 2.5 hours. The two phases were separated and the organic phase was dried (Na2SO4), and concentrated in vacuo. The residue was purified by preparative TLC and eluted with 5% ethylacetate in hexane to yield 3-methyl-4-hydroxy-5-propyl-7-fluorobenzofuran (62 mg; 75%), identical to the product obtained from the cyclisation reaction described above in step f.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05087638
Source datasetuspto-grants-1992_02
ORD IDord-e59f5ea6d62946e4acbb858c8a9c4c7f
Source noteuspto-grants-1992_02