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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Xylene | HCID 7809 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 4-Ethenylphenyl acetate | HCID 75821 | — |
| Reactant | 3,5-Bis(methoxymethoxy)benzoyl chloride | HCID 59301730 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | 1,3-BIS(2,6-DIISOPROPYLPHENYL)imidazoLIDINIUM-CHLORIDE | HCID 18454782 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4'-Acetoxy-3,5-bis(methoxymethoxy)stilbene | HCID 67170243 | 59% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07714161B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-7257de764c6d48af958cc133ae028272 |
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| Source note | uspto-grants-2010_05 |
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