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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432324Generated: November 2, 2026

N-Benzylidene-4-bromoaniline → N-(4-Bromophenyl)-N-(1-phenylethyl)amine

https://huagongshe.com/reaction/432324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Benzylidene-4-bromoanilineHCID 262176—
ReactantHCID 178418348HCID 178418348—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductN-(4-Bromophenyl)-N-(1-phenylethyl)amineHCID 12174320—

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a solution of N-(4-bromophenyl)-N-(1-phenylmethylidene)amine (1.0 g, 0.00385 mol) in toluene (30 mL) cooled to −78° C., a 1.4M solution of methyl lithium in diethyl ether (5.5 mL) was added dropwise keeping the temperature below −75° C. The solution was warmed up to −40° C. and stirred at this temperature under an atmosphere of nitrogen for 3 hours. The reaction mixture was quenched by a dropwise addition of water and the layers were separated. The organic phase was washed with brine (50 mL), dried with magnesium sulfate and concentrated under reduced pressure to yield N-(4-bromophenyl)-N-(1-phenylethyl)amine (1.03 g, 0.00373 mol) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660744B1
Source datasetuspto-grants-2003_12
ORD IDord-e499d1564ee44a958f9479b62bfb4acf
Source noteuspto-grants-2003_12