HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78880Generated: October 27, 2026
P-Xylene → 3,5-Diacetoxy-4'-fluorostilbene
https://huagongshe.com/reaction/78880
Participants
| Role | Name | HCID | Charge |
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| Reactant | P-Xylene | HCID 7809 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 4-Fluorostyrene | HCID 67883 | — |
| Reactant | (3-Acetyloxy-5-carbonochloridoylphenyl) acetate | HCID 11368883 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | 1,3-BIS(2,6-DIISOPROPYLPHENYL)imidazoLIDINIUM-CHLORIDE | HCID 18454782 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3,5-Diacetoxy-4'-fluorostilbene | HCID 68740790 | 73.2% |
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) δ 7.45 (dd, 2H), 7.11-6.91 (m, 6H), 6.82 (t, J=1.95 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841477B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-1d549d6ad7be434096e133f0f8199bef |
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| Source note | uspto-grants-2014_09 |
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