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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883971Generated: October 25, 2026

Ethanol → 3-(3-Bromo-phenoxymethyl)-phenylamine

https://huagongshe.com/reaction/883971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Nitro-3-(3-bromo-phenoxymethyl)-benzeneHCID 28369541—
CatalystIronHCID 23925—
SolventTetrahydrofuranHCID 8028—
Product3-(3-Bromo-phenoxymethyl)-phenylamineHCID 2011295997%

Reaction Steps

To a solution of the product from Example 74A (1.64 g, 5.32 mmol), iron powder (1.49 g, 26.62 mmol) and ammonium chloride (430 mg, 7.98 mmol) in a mixture of tetrahydrofuran (20 mL), water (6 mL) and ethanol (20 mL) was heated to reflux for 3 hours. The mixture was cooled to room temperature, filtered through a pad of celite, which was washed with ethanol and the resultant filtrate concentrated under vacuum. The material was then dissolved in water (50 mL) and extracted with ethyl acetate (50 mL), the organic layer dried and concentrated under vacuum to provide the title compound as a yellow oil (1.43 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236950B2
Source datasetuspto-grants-2012_08
ORD IDord-61b3a1cfcfd144d19e955f8f12e784de
Source noteuspto-grants-2012_08