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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975739Generated: October 30, 2026

Dichloromethane → 1-(4-Chlorobenzyl)-1-[4-(pyrid-2-ylmethoxy)phenyl] hydrazine

https://huagongshe.com/reaction/1975739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(Pyrid-2-ylmethoxy)phenylhydrazineHCID 19098339—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
Product1-(4-Chlorobenzyl)-1-[4-(pyrid-2-ylmethoxy)phenyl] hydrazineHCID 19098330—

Reaction Steps

4-(Pyrid-2-ylmethoxy)phenylhydrazine (66.2 g; 308 mmol), prepared as in step 3, was added to a solution of 86 mL diisopropylethylamine and 900 mL dichloromethane. 4-Chlorobenzyl chloride (74.4 g; 462 mmol) and tetrabutylammonium bromide (29.8 g; 92.4 mmol) and an additional 100 mL dichloromethane were added and the reaction was stirred at ambient temperature for 24 hours. The reaction mixture was diluted with water and the layers were separated. The aqueous layer was extracted with dichloromethane. The combined organics were dried over magnesium sulfate and concentrated. The residue was washed with 9:1 diethyl ether, methanol to afford 1-(4-chlorobenzyl)-1-[4-(pyrid-2-ylmethoxy)phenyl] hydrazine as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05288743
Source datasetuspto-grants-1994_02
ORD IDord-42eb282e965041b39511e86f250fb8c1
Source noteuspto-grants-1994_02