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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105286Generated: November 1, 2026

1-Bromo-2,4-dimethyl-3-nitrobenzene → 3-Bromo-2,6-dimethylaniline

https://huagongshe.com/reaction/2105286

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2,4-dimethyl-3-nitrobenzeneHCID 2753380—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
Product3-Bromo-2,6-dimethylanilineHCID 12792330—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of crude 1-bromo-2,4-dimethyl-3-nitrobenzene (0.58 g, 2.9 mmol) in glacial acetic acid (12 mL) was added iron powder (0.65 g, 11.6 mmol). The mixture was stirred rapidly at 80° C. under nitrogen for 2 hours. Upon completion, the mixture was cooled, diluted with diethyl ether and extracted with aqueous sodium hydroxide solution (2N). The organic layer was dried over sodium sulfate, decanted and concentrated under reduced pressure to give 3-bromo-2,6-dimethylphenylamine as a yellow oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579340B2
Source datasetuspto-grants-2009_08
ORD IDord-e7713b99876e4fbba8fd1277b8d56e53
Source noteuspto-grants-2009_08