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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609218Generated: October 25, 2026

1-Chloro-4-(chloromethyl)benzene → 1-(4-Chlorobenzyl)-1-(4-methoxyphenyl)hydrazine

https://huagongshe.com/reaction/1609218

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantDiisopropylamineHCID 7912—
Reactant4-Methoxyphenylhydrazine hydrochlorideHCID 2723904—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDichloromethaneHCID 6344—
Product1-(4-Chlorobenzyl)-1-(4-methoxyphenyl)hydrazineHCID 1498056472%

Reaction Steps

To a suspension under N2 of 4-methoxyphenylhydrazine hydrochloride (41 g, 230 mmol) in methylene chloride (1000 ml) were added diisopropylamine (79.8 g, 612 mmol), 4-chlorobenzyl chloride (40.25 g, 250 mmol) and tetrabutylammonium bromide (22.8 g, 70 mmol), and the resulting mixture was stirred at room temperature for 48 hours. The reaction mixture was then washed with water and brine, dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by chromatography on silica gel (2.5% methanol/methylene chloride), followed by washing of the solid with 10% ethyl ether in hexane and drying in vacuo to provide 43.5 g of 1-(4-chlorobenzyl)-1-(4-methoxyphenyl)hydrazine. mp.55° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05399699
Source datasetuspto-grants-1995_03
ORD IDord-033cb681b4324a7a82dfee28727d1660
Source noteuspto-grants-1995_03