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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323982Generated: October 29, 2026

4-(2-Bromoethoxy)benzonitrile → N-[2-(4-cyanophenoxy)ethyl]phthalimide

https://huagongshe.com/reaction/323982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Bromoethoxy)benzonitrileHCID 2452212—
ReactantPhthalimide potassium saltHCID 24194345—
SolventDimethylformamideHCID 6228—
ProductN-[2-(4-cyanophenoxy)ethyl]phthalimideHCID 8150643—

Reaction Conditions

Temperature95 °C

Reaction Steps

4-(2-Bromoethoxy)benzonitrile (7.3 g) was reacted with potassium phthalimide (5.98 g) in DMF (35 ml) by heating at 95° C. for 3 hours. The N-[2-(4-cyanophenoxy) ethyl]phthalimide obtained after extractive workup (7.30 g) was suspended in IMS (350 ml) and treated with hydrazine hydrate (6.25 g). The mixture was stirred for 22 hours and filtered. The solid obtained was washed with IMS and the combined filtrate and washings were evaporated to dryness. Water was added to this residue and the mixture basified with 10M sodium hydroxide solution. The mixture was extracted with dichloromethane to give 4-(2-aminoethoxy)benzonitrile as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06215001B1
Source datasetuspto-grants-2001_04
ORD IDord-0e7042f321da4170ac9caa9114453ff0
Source noteuspto-grants-2001_04