HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78878Generated: October 25, 2026
P-Xylene → 3,5-Difluoro-4'-acetoxystilbene
https://huagongshe.com/reaction/78878
Participants
| Role | Name | HCID | Charge |
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| Reactant | P-Xylene | HCID 7809 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 4-Ethenylphenyl acetate | HCID 75821 | — |
| Reactant | 3,5-Difluorobenzoyl chloride | HCID 145600 | — |
| 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-Difluoro-4'-acetoxystilbene | HCID 68742160 | 74.4% |
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
| 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-999fdb07a7264857b0b22f06af7d7172 |
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| Source note | uspto-grants-2014_09 |
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