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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751627Generated: October 28, 2026

6-Bromo-1-nitronaphthalen-2-amine → 6-Bromonaphthalene-1,2-diamine

https://huagongshe.com/reaction/1751627

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-1-nitronaphthalen-2-amineHCID 21807185—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product6-Bromonaphthalene-1,2-diamineHCID 2209707189.4%

Reaction Steps

To a mixture of 6-bromo-1-nitronaphthalen-2-amine (11.6 g, 43.4 mmol) in ethanol (430 mL) under argon was added Raney Nickel (˜5 g, NOTE: no effort was made to remove the water from the nickel). Hydrogen gas was bubbled through the reaction mixture for 2 minutes. The reaction was stirred under an atmosphere of hydrogen at room temperature. After 16 hours, the Raney Nickel was removed by filtration over Celite and rinsed with ethyl acetate. The filtrate was thoroughly concentrated to yield 6-bromonaphthalene-1,2-diamine (9.2 g, 88% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156823B2
Source datasetuspto-grants-2015_10
ORD IDord-b11ee7811d074a498a47252296fd488e
Source noteuspto-grants-2015_10