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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236341Generated: October 30, 2026

P-Xylene → 3,5-Diacetoxy-4'-fluorostilbene

https://huagongshe.com/reaction/2236341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-XyleneHCID 7809—
Reactant4-MethylmorpholineHCID 7972—
Reactant4-FluorostyreneHCID 67883—
Reactant(3-Acetyloxy-5-carbonochloridoylphenyl) acetateHCID 11368883—
Catalystpalladium(II) acetateHCID 167845—
Catalyst1,3-BIS(2,6-DIISOPROPYLPHENYL)imidazoLIDINIUM-CHLORIDEHCID 18454782—
SolventEthyl AcetateHCID 8857—
Product3,5-Diacetoxy-4'-fluorostilbeneHCID 6874079073.2%

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-diacetoxybenzoyl chloride (1.28 g, 5 mmol), 4-fluorostyrene (0.73 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 (1.15 g, 73%) as white solid. Data are: 1H NMR (CDCl3, 300 MHz) δ7.45 (dd, 2H), 7.11-6.91 (m, 6H), 6.82 (t, J=1.95 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714161B2
Source datasetuspto-grants-2010_05
ORD IDord-b61bc0d6d9a84e6888d16aba15ff597c
Source noteuspto-grants-2010_05