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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270605Generated: October 25, 2026

4-(3-Bromo-4-methoxyphenoxy)-3,5-dimethylnitrobenzene → 4-(3-Bromo-4-methoxy-phenoxy)-3,5-dimethyl-phenylamine

https://huagongshe.com/reaction/1270605

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-Bromo-4-methoxyphenoxy)-3,5-dimethylnitrobenzeneHCID 22339728—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product4-(3-Bromo-4-methoxy-phenoxy)-3,5-dimethyl-phenylamineHCID 2233950294%

Reaction Steps

A mixture of the title product of Step A (5.0 g) and 10% palladium on carbon (0.6 g) in ethyl acetate (100 ml) was hydrogenated at 50 psi for 3 h. The reaction was filtered through Celite and concentrated to afford the title compound of Step B as a yellow solid (4.3 g). MS (APCI+) Calc: 321; Found 322 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202275B2
Source datasetuspto-grants-2007_04
ORD IDord-b61df12010b442ab977621dfdc206ed3
Source noteuspto-grants-2007_04