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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712067Generated: November 3, 2026

Sodium borohydride → HCID 59205225, compound

https://huagongshe.com/reaction/1712067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59205195HCID 59205195—
SolventEthanolHCID 702—
ProductHCID 59205225HCID 59205225—

Reaction Steps

4-(3-Formyl-phenyl)-7-trifluoromethyl-quinoline-3-carboxylic acid ethyl ester (16 mg, 0.034 mmol) was dissolved in ethanol (1 mL) and treated with sodium borohydride (15 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 dried over sodium sulfate, concentrated and the residue purified by to column chromatography eluted with 30% ethyl acetate to yield 4-(3-hydroxymethyl-phenyl)-7-trifluoromethyl-quinoline-3-carboxylic acid ethyl ester as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790895B2
Source datasetuspto-grants-2010_09
ORD IDord-26085792d7e14c5cacfe31080d2858e8
Source noteuspto-grants-2010_09