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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418782Generated: October 27, 2026

Chloroform → 4-(Chlorodiphenylmethyl)pyridine

https://huagongshe.com/reaction/2418782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactantalpha,alpha-Diphenyl-4-pyridinemethanolHCID 74177—
SolventBenzeneHCID 241—
Product4-(Chlorodiphenylmethyl)pyridineHCID 13215895—

Reaction Steps

92.1 g (0.353 mol) of diphenyl(4-pyridyl)methyl alcohol recrystallized from chloroform and 800 ml of simple-distillation benzene were charged in a 2-l three-necked flask provided with a stirrer and reflux condenser. The mixture was treated at 50° C. to form a suspension. 29.6 ml (0.407 mol) of thionyl chloride was poured in the suspension and the mixture was stirred under reflux for 1 h. The resulting solution was cooled to room temperature. 72.5 ml (0.522 mol) of triethylamine was added thereto and the mixture was stirred for 7 h. The reaction solution was filtered and the filtrate was concentrated to obtain crude diphenyl(4-pyridyl)methyl chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04473690
Source datasetuspto-grants-1984_09
ORD IDord-0e65485d873741038106db271a2c4286
Source noteuspto-grants-1984_09