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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067236Generated: November 2, 2026

Sodium borohydride → (1-Chloroisoquinolin-5-yl)methanol

https://huagongshe.com/reaction/1067236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-Chloroisoquinoline-5-carbaldehydeHCID 21192467—
SolventMethanolHCID 887—
Product(1-Chloroisoquinolin-5-yl)methanolHCID 2119247076.9%

Reaction Steps

A solution of 1-chloro-5-isoquinolinecarboxaldehyde (308 mg, 1.6 mmol) and sodium borohydride (NaBH4) (68 mg, 1.8 mmol) in MeOH (6 mL) was stirred at room temperature for 2 h. The reaction was quenched with water (2 mL) and concentrated in vacuo. The residue was suspended in CH2Cl2, washed with water, with brine and then dried over MgSO4 and evaporated. The residue was purified by column chromatography upon silica gel using hexanes-EtOAc (80:20 to 50:50) as eluant to give 1-chloro-5-(hydroxymethyl)isoquinoline (240 mg, 1.23 mmol) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248738B1
Source datasetuspto-grants-2001_06
ORD IDord-b3d412980bae4d8eaeeb27c270d38927
Source noteuspto-grants-2001_06