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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120121Generated: October 28, 2026

3,5-Dichloro-4-pyridinecarboxaldehyde → (3,5-Dichloropyridin-4-yl)methanol

https://huagongshe.com/reaction/2120121

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dichloro-4-pyridinecarboxaldehydeHCID 2762988—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(3,5-Dichloropyridin-4-yl)methanolHCID 1785521978%

Reaction Steps

A solution of 3,5-dichloropyridine-4-carboxaldehyde (1.34 g, 7.6 mmol) in MeOH (10 ml) was treated with NaBH4 (0.29 g, 7.6 mmol) and stirred at room temperature for 2 h. The reaction was quenched with water (5 ml) and concentrated in vacuo. The residue was partitioned between EtOAc (20 ml) and 10% HCl (10 ml). The aqueous layer was extracted with EtOAc and the combined organic extracts washed with 10% NaHCO3 solution, dried (MgSO4) and concentrated in vacuo to give the title compound as a white solid (1.05 g, 78%): δH (CDCl3) 8.52 (2H, s), 4.94 (2H, br. s), 2.28 (1H, br. s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689781B2
Source datasetuspto-grants-2004_02
ORD IDord-83f7bd91d6ed4d4c9f761c8457fd1ad2
Source noteuspto-grants-2004_02