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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751626Generated: October 28, 2026

Ammonia → 6-Bromo-1-nitronaphthalen-2-amine

https://huagongshe.com/reaction/1751626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
Reactant6-Bromo-2-methoxy-1-nitronaphthaleneHCID 22097187—
SolventMethanolHCID 887—
Product6-Bromo-1-nitronaphthalen-2-amineHCID 2180718595%

Reaction Conditions

Temperature130 °C

Reaction Steps

6-bromo-2-methoxy-1-nitronaphthalene (12.6 g, 44.7 mmol), dimethylformamide (25.6 mL) and 7N NH3 solution in MeOH (128 mL, purchased from Sigma Aldrich) were combined in a Parr bomb. The bomb was heated in a lab oven at 130° C. After 48 hours, the reactor was removed from the oven and cooled to room temperature. The contents of the bomb were transferred to a glass round bottom flask. The bomb was thoroughly rinsed with dichloromethane and methanol, and the rinsings added to the flask. The contents of the flask were thoroughly concentrated on a rotary evaporator, leaving a brown solid. Water (200 mL) was added to the flask and the resulting suspension was agitated with a stir bar for 30 minutes. The resulting light brown powder was isolated by filtration, rinsing a few times with water. The filter cake was air dried over night to yield 6-bromo-1-nitronaphthalen-2-amine (11.6 g, >95% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156823B2
Source datasetuspto-grants-2015_10
ORD IDord-9149a1d131d54949801440a2161045ca
Source noteuspto-grants-2015_10