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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082159Generated: October 31, 2026

Thionyl Chloride → 4-(4-Chlorobutyl)pyridine

https://huagongshe.com/reaction/2082159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant4-PyridinebutanolHCID 2784655—
SolventChloroformHCID 6212—
Product4-(4-Chlorobutyl)pyridineHCID 10953941—

Reaction Steps

A solution of 4-(4-pyridinyl)-1-butanol (Mayer J. M. and Testa, B., -Helv. Chim. Acta 65, pages 1868-1884 (1982) (4.20 g, 27.7 mmol) in 30 mL of chloroform is cooled to 0° C. and treated with thionyl chloride (6.60 g, 55.54 mmol) in 30 mL of chloroform. The reaction is allowed to warm to room temperature over 15 hours. The volatiles are removed in vacuo. The residue is cooled to 0° C. and treated with 50 mL of cold 10% sodium hydroxide solution and the mixture is extracted with three 100-mL portions of chloroform. The combined organic extracts are dried over sodium sulfate and the solvents are removed under reduced pressure to give 4.25 g of 4-(4-pyridinyl)-1-butylchloride as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05187280
Source datasetuspto-grants-1993_02
ORD IDord-a078dbc6d4b34c3d829d2c26b6dddf5a
Source noteuspto-grants-1993_02