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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236329Generated: October 25, 2026

P-Xylene → 4'-Acetoxy-3,5-bis(methoxymethoxy)stilbene

https://huagongshe.com/reaction/2236329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-XyleneHCID 7809—
Reactant4-MethylmorpholineHCID 7972—
Reactant4-Ethenylphenyl acetateHCID 75821—
Reactant3,5-Bis(methoxymethoxy)benzoyl chlorideHCID 59301730—
CatalystPalladiumHCID 23938—
Catalyst1,3-BIS(2,6-DIISOPROPYLPHENYL)imidazoLIDINIUM-CHLORIDEHCID 18454782—
SolventEthyl AcetateHCID 8857—
Product4'-Acetoxy-3,5-bis(methoxymethoxy)stilbeneHCID 6717024359%

Reaction Conditions

Temperature120 °C

Reaction Steps

A 50 mL round bottom flask was charged with p-xylene (20 mL), Pd II catalyst (22.5 mg, 0.1 mmol), 1,3-bis-(2,6-diisopropylphenyl) imidazolinium chloride (42.7 mg, 0.1 mmol), 3,5-bis(methoxymethoxy)benzoyl chloride (2.42 g, 10 mmol), 4-acetoxystyrene (1.94 g, 12 mmol), and N-methyl morpholine (1.38 g, 12 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 (2.1 g, 59%) as white solid. Data are: 1H NMR (CDCl3, 300 MHz) δ 7.48 (d, 2H), 7.08-6.93 (m, 4H), 6.86 (d, 2H), 6.66 (t, 1H), 5.19 (s, 4H), 3.50 (s, 6H), 2.30 (s, 3H); 13C NMR (CDCl3, 75 MHz) δ 169.5, 158.7, 150.3, 139.5, 135.0, 128.7, 128.5, 127.6, 121.9, 108.0, 104.5, 94.6, 56.2, 21.2; HRMS (EI+) found 358.1409 M+, calcd 358.1416 for C20H22O6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714161B2
Source datasetuspto-grants-2010_05
ORD IDord-7257de764c6d48af958cc133ae028272
Source noteuspto-grants-2010_05