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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399822Generated: November 2, 2026

Ammonium Chloride → 5-bromo-N-(4-methoxybenzyl)benzene-1,2-diamine

https://huagongshe.com/reaction/1399822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant5-bromo-N-(4-methoxybenzyl)-2-nitroanilineHCID 65341673—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product5-bromo-N-(4-methoxybenzyl)benzene-1,2-diamineHCID 6534334382%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 5-bromo-N-(4-methoxybenzyl)-2-nitroaniline (750 mg, crude) in EtOH (8 mL) and H2O (8 mL) was added Fe powder (766 mg, 13.7 mmol) and ammonium chloride (733 mg, 13.7 mmol). The mixture was stirred at 60° C. for 4 h then filtered and the filtrate was concentrated to remove EtOH. The residue was then diluted with water and extracted with EtOAc. The organic layer was concentrated to give the desired product (550 mg, crude, 82% yield) with the crude product being used in next step without further purification. LCMS (m/z): 308.1 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906900B2
Source datasetuspto-grants-2014_12
ORD IDord-78cf8c19c3e84b228e491f26257970a6
Source noteuspto-grants-2014_12