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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699836Generated: November 2, 2026

HCID 22388405, compound → HCID 22387947, compound

https://huagongshe.com/reaction/1699836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22388405HCID 22388405—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22387947HCID 2238794794.8%

Reaction Steps

3-(2,4-Dichlorobenzoyl)-5-(methoxycarbonyl)-2-methylbenzo[b]furan (0.84 g, 2.31 mmol) was dissolved in tetrahydrofuran (20 ml) and a solution (1.0 M, 5 ml, 5 mmol) of a borane-tetrahydrofuran complex in tetrahydrofuran was added. The mixture was stirred at room temperature for 30 min and then at 50° C. for 2 hr. The reaction mixture was concentrated under reduced pressure and a saturated aqueous ammonium chloride solution was added to the residue. The mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The desiccant was filtered off and the filtrate was concentrated under reduced pressure to give the objective compound (0.8 g) as a colorless oil. This crude product was used in the next reaction as it was.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06348474B1
Source datasetuspto-grants-2002_02
ORD IDord-6ada02c0544f4e7584ceb17bbf827cb9
Source noteuspto-grants-2002_02