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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77498Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/77498

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt1-Chloro-4-(chloromethyl)benzeneHCID 7723—
EduktDiisopropylethylamineHCID 81531—
Edukt4-Methoxyphenylhydrazine hydrochlorideHCID 2723904—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDichloromethaneHCID 6344—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt1-(4-Chlorobenzyl)-1-(4-methoxyphenyl)hydrazine hydrochlorideHCID 18947569—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841295B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-aa3a6fcfab7f4ae288aee51a9ed94b8b
Quellennotizuspto-grants-2014_09