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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242106Generated: October 31, 2026

Sodium borohydride → HCID 11668580, compound

https://huagongshe.com/reaction/2242106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 11603785HCID 11603785—
SolventEthanolHCID 702—
ProductHCID 11668580HCID 11668580—

Reaction Steps

4-(5-Formyl-2-methoxy-phenyl)-7-trifluoromethyl-quinoline-3-carboxylic acid ethyl ester (30 mg, 0.074 mmol) was dissolved in ethanol (1 mL) and treated with sodium borohydride (26 mg) in one portion. After stirring at room temperature for 15 min, the reaction mixture was quenched with an aqueous solution of ammonium chloride. The reaction mixture was then extracted with ethyl acetate and the organic layer was dried over sodium sulfate, concentrated. The crude compound was purified by column chromatography eluted with 30% ethyl acetate to yield 4-(5-hydroxymethyl-2-methoxy-phenyl)-7-trifluoromethyl-quinoline-3-carboxylic acid ethyl ester as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671065B2
Source datasetuspto-grants-2010_03
ORD IDord-3a8aacc5a93b44809f7dfb859cf39c60
Source noteuspto-grants-2010_03