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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036836Generated: October 26, 2026

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

https://huagongshe.com/reaction/1036836

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 (3.7 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 numberUS08546431B2
Source datasetuspto-grants-2013_10
ORD IDord-03063b24078a4a1bba6b8478f4e8243a
Source noteuspto-grants-2013_10