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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1849997Generated: October 25, 2026

Sodium borohydride → (5-Bromoquinolin-8-yl)methanol

https://huagongshe.com/reaction/1849997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-Bromoquinoline-8-carboxaldehydeHCID 16414243—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product(5-Bromoquinolin-8-yl)methanolHCID 72183353100.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-bromoquinoline-8-carbaldehyde ([CAS 885267-41-7] 423 mg, 1.79 mmol) in MeOH (5 mL) and THF (10 mL) was added sodium borohydride (68 mg, 1.79 mmol) at 0° C. After stirring at 0° C. for 30 min, the reaction mixture was quenched with a saturated aqueous ammonium chloride solution. The mixture was extracted with ethyl acetate. The combined organic layers were washed with brine, dried with magnesium sulfate and concentrated under reduced pressure to give rise to 430 mg of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957051B2
Source datasetuspto-grants-2015_02
ORD IDord-e0417a9ab70e4cf1a15f473ae666edb6
Source noteuspto-grants-2015_02