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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956879Generated: November 1, 2026

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

https://huagongshe.com/reaction/1956879

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 numberUS05780642
Source datasetuspto-grants-1998_07
ORD IDord-584f0dd9d66e41af9d545e827a58a037
Source noteuspto-grants-1998_07