Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072814Generated: November 4, 2026

HCID 22388405, compound → HCID 22387947, compound

https://huagongshe.com/reaction/1072814

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 numberUS06911469B2
Source datasetuspto-grants-2005_06
ORD IDord-37487f9aceb1444888fc301cb0fa5c06
Source noteuspto-grants-2005_06