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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236339Generated: October 31, 2026

P-Xylene → 3,5-Difluoro-4'-acetoxystilbene

https://huagongshe.com/reaction/2236339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-XyleneHCID 7809—
Reactant4-MethylmorpholineHCID 7972—
Reactant4-Ethenylphenyl acetateHCID 75821—
Reactant3,5-Difluorobenzoyl chlorideHCID 145600—
Catalystpalladium(II) acetateHCID 167845—
Catalyst1,3-BIS(2,6-DIISOPROPYLPHENYL)imidazoLIDINIUM-CHLORIDEHCID 18454782—
SolventEthyl AcetateHCID 8857—
Product3,5-Difluoro-4'-acetoxystilbeneHCID 6874216074.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A 25 mL round bottom flask was charged with p-xylene (10 mL), Pd(OAc)2 (11.3 mg, 0.05 mmol), 1,3-bis-(2,6-diisopropylphenyl) imidazolinium chloride (21.4 mg, 0.05 mmol), 3,5-difluorobenzoyl chloride (0.89 g, 5 mmol), 4-acetoxystyrene (0.97 g, 6 mmol), and N-methyl morpholine (0.69 g, 6 mmol). The mixture was stirred at 120° C. for 3.5 h under nitrogen atmosphere. Then it was cooled to room temperature and EtOAc was added and filtered. The filtrate was washed with brine and dried over Na2SO4. Then it was filtered and purified via flash chromatography and gave the product (1.02 g, 74%) as white solid. Data are: 1H NMR (CDCl3, 300 MHz) δ 7.51 (d, J=8.4 Hz, 2H), 7.12-6.97 (m, 6H), 6.70 (t, 1H), 2.31 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714161B2
Source datasetuspto-grants-2010_05
ORD IDord-1920f297bfc04dc693f3e102cbb39d83
Source noteuspto-grants-2010_05