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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727857Generated: November 4, 2026

Ethanol → HCID 23022688, compound

https://huagongshe.com/reaction/1727857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHCID 9932979HCID 9932979—
ReactantHCID 178418435HCID 178418435—
SolventWaterHCID 962—
ProductHCID 23022688HCID 2302268897%

Reaction Steps

[4-(Tert-butyl)phenyl]{4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-methanone (111 mg) and sodium boron hydride (76 mg) were added to ethanol (15 ml), and the mixture was stirred at room temperature for 3 hr. Water was added to the reaction solution, and the mixture was extracted with chloroform. The chloroform layer was dried over anhydrous sodium sulfate. Chloroform was removed by evaporation under the reduced pressure to give a crude which was then purified by thin-layer chromatography on silica gel using chloroform/ethyl acetate for development to give (4-tert-butylphenyl)-[4-(6,7-dimethoxy-4-quinolyloxy)phenyl]methanol (108 mg, yield 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495104B2
Source datasetuspto-grants-2009_02
ORD IDord-38b38a2dcd8e48be9b68f0547770587c
Source noteuspto-grants-2009_02