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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192490Generated: November 1, 2026

Sodium borohydride → 1-[5-Chloro-8-(2-fluorophenyl)quinolin-7-yl]ethanol

https://huagongshe.com/reaction/1192490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-[5-Chloro-8-(2-fluorophenyl)quinolin-7-yl]ethanoneHCID 67249535—
SolventMethanolHCID 887—
Product1-[5-Chloro-8-(2-fluorophenyl)quinolin-7-yl]ethanolHCID 67248433—

Reaction Steps

To a mixture of 1-[5-chloro-8-(2-fluorophenyl)quinolin-7-yl]ethanone (0.032 g, 0.11 mmol) in methanol (0.3 mL) was added sodium tetrahydroborate (0.0040 g, 0.11 mmol). The reaction was stirred at room temperature for 1 hour, quenched with saturated sodium bicarbonate and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, and then concentrated to dryness under reduced pressure. The resulting residue was used in next step (33 mg, 100%). LCMS calculated for C17H14ClFNO(M+H)+: m/z=302.1; found: 302.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-c7520f0704c043368ae4b9e7e47c048e
Source noteuspto-grants-2014_03