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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959542Generated: November 1, 2026

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

https://huagongshe.com/reaction/1959542

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dichloro-4-pyridinecarboxaldehydeHCID 2762988—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product(3,5-Dichloropyridin-4-yl)methanolHCID 17855219—

Reaction Steps

NaBH4 (0.838 g, 22.2 mmol) was added to a stirred solution of 3,5-dichloro-pyridine-4-carbaldehyde (3.0 g, 17 mmol) in ethanol (40 mL). After stirring for 35 min at room temperature, the reaction mixture was concentrated in vacuo, the residue was redissolved in ethyl acetate (200 mL) and washed with water (50 mL). The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo to give the title compound. MS (m/z): 178.1 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410134B2
Source datasetuspto-grants-2013_04
ORD IDord-60df8377dd3240d493043d9ef0f738b5
Source noteuspto-grants-2013_04