Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712066Generated: November 4, 2026

Sodium borohydride → HCID 11668580, compound

https://huagongshe.com/reaction/1712066

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 numberUS07790895B2
Source datasetuspto-grants-2010_09
ORD IDord-e89532d587a84b43968ebe1802edab2c
Source noteuspto-grants-2010_09