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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77498Generated: October 25, 2026

Hydrochloric Acid → 1-(4-Chlorobenzyl)-1-(4-methoxyphenyl)hydrazine hydrochloride

https://huagongshe.com/reaction/77498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Methoxyphenylhydrazine hydrochlorideHCID 2723904—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product1-(4-Chlorobenzyl)-1-(4-methoxyphenyl)hydrazine hydrochlorideHCID 18947569—

Reaction Steps

A solution of 4-Methoxyphenylhydrazine hydrochloride (10.0 g, 57.3 mmol), 4-chlorobenzylchloride (9.2 g, 57.2 mmol), tetrabutylammonium bromide (30.7 g, 11.5 mmol), and diisopropylethylamine (20 mL, 115 mmol) in CH2Cl2 (250 mL) was stirred at room temperature for several days. The reaction mixture was diluted with water and the organic layer was dried over MgSO4, filtered, and concentrated. The residue was taken up in toluene (200 mL) and diethyl ether (100 mL), and 1 equivalent of 4N HCl in dioxane was added at 0° C. The mixture was stirred at room temperature for 2 hours, and then evaporated to dryness to give the desired product (C-1; X═Cl) as a purple solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841295B2
Source datasetuspto-grants-2014_09
ORD IDord-aa3a6fcfab7f4ae288aee51a9ed94b8b
Source noteuspto-grants-2014_09