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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378642Generated: October 30, 2026

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

https://huagongshe.com/reaction/378642

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 numberUS06031109
Source datasetuspto-grants-2000_02
ORD IDord-cff29d1525084a3e9555754898563020
Source noteuspto-grants-2000_02