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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074580Generated: October 30, 2026

Pyridine → 3-Phenoxybenzyl chloride

https://huagongshe.com/reaction/1074580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
Reactant3-Phenoxybenzyl alcoholHCID 26295—
SolventChloroformHCID 6212—
Product3-Phenoxybenzyl chlorideHCID 9329196%

Reaction Steps

To a solution of 200 g. of m-phenoxy-benzyl alcohol in 1 liter of dry chloroform 2 ml. of pyridine are added and a solution of 142.8 g. thionyl-chloride in 150 ml. of chloroform is added dropwise under cooling with ice water. When the addition is completed the cooling is terminated and the solution is allowed to warm up to room temperature under stirring and the temperature is maintained under stirring until the vigorous gas evolution ceases. The mixture is then boiled under stirring until the gas evolution ceases completely. The solution is then poured into 2 liters of cold water, the chloroform layer is separated and the aqueous layer is shaken out in 400 ml. of chloroform. The combined chloroform solutions are washed once with water and dried above sodium sulphate. The drying agent is filtered off and chloroform is distilled off; thus 210 g. (96%) of m-phenoxy-benzyl chloride are obtained, which can be distilled at 128° to 130° C. at a pressure of 0.3 mmHg. Substantially no forerun and residue are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04393008
Source datasetuspto-grants-1983_07
ORD IDord-cec340a9ef0c476f9186e57dfb0e5378
Source noteuspto-grants-1983_07