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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193964Generated: November 2, 2026

Pyridine → 5-(Chloromethyl)pyridine-2-carbonitrile

https://huagongshe.com/reaction/1193964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant2-Cyano-5-hydroxymethylpyridineHCID 12251966—
SolventTolueneHCID 1140—
Product5-(Chloromethyl)pyridine-2-carbonitrileHCID 1440512350.5%

Reaction Steps

2-Cyano-5-hydroxymethylpyridine (13.4 g) and pyridine (8.7 g) were dissolved in toluene (150 ml), and a solution of p-toluenesufonyl chloride (19.1 g) in toluene (50 ml) was added dropwise at room temperature to the solution. After the addition, the mixture was gradually heated, and stirred at 70° to 80° C. for 4 hours. The reaction mixture was cooled to room temperature, and washed with water. The organic layer was dried. Toluene was distilled off under reduced pressure. The residue was purified by silica gel column chromatography to give 2-cyano-5-pyridylmethyl chloride (7.7 g) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04812454
Source datasetuspto-grants-1989_03
ORD IDord-0b033bdf95c3497986859f01efe950f0
Source noteuspto-grants-1989_03