Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885085Generated: October 30, 2026

4-Methoxystyrene → HCID 11579752, compound

https://huagongshe.com/reaction/885085

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxystyreneHCID 12507—
Reactant4-Bromo-3-nitroanisoleHCID 79288—
ReactantDiisopropylethylamineHCID 81531—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-(Di-tert-butylphosphino)biphenylHCID 2734215—
SolventAcetonitrileHCID 6342—
ProductHCID 11579752HCID 1157975279.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 2-bromo-5-methoxynitrobenzene (5 g, 21.6 mmol) in dry acetonitrile (60 mL) were added 4-methoxystyrene (3.04 g, 22.6 mmol), N,N-diisopropylethylamine (8.36 g, 64.6 mmol), biphenyl-2-yl-di-t-butyl phosphine (385 mg, 1.3 mmol) and palladium acetate (290 mg, 1.3 mmol). The resulting mixture was heated at 80° C. overnight under N2. The reaction mixture was cooled to room temperature and partitioned between ethyl acetate and water. The organic layer was separated, washed with water, brine, and dried over magnesium sulfate. Concentration under reduced pressure gave the crude product which was purified by column chromatography using ethyl acetate in hexane (5%-10%) to give the protected nitro-stilbene (4.4 g, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242144B2
Source datasetuspto-grants-2012_08
ORD IDord-0d63bf7393654a1a8136e5fe0fd2b3d5
Source noteuspto-grants-2012_08