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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630293Generated: October 27, 2026

Water → (3-Chloropyridin-4-yl)methanol

https://huagongshe.com/reaction/630293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Chloro-4-pyridinecarboxaldehydeHCID 2762995—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(3-Chloropyridin-4-yl)methanolHCID 1274246696%

Reaction Steps

To a 0° C. solution of 3-chloropyridine-4-carbaldehyde (1.08 g, 7.5 mmol) in anhydrous methanol (75 mL) was added sodium borohydride (405 mg, 10.7 mmol). The reaction mixture was stirred at room temperature for 1.5 hours. Water (75 mL) was added, and the reaction mixture was evaporated. The resultant residue was extracted with EtOAc (3×50 mL). The organic extracts were combined, washed with brine (2×100 mL), dried over MgSO4, filtered, evaporated, and dried in vacuo, affording (3-chloropyridin-4-yl)methanol (1.0 g, 96%). The product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315521B2
Source datasetuspto-grants-2016_04
ORD IDord-0a7118d7ebd04760ac542c26bd01f4f7
Source noteuspto-grants-2016_04