HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007349Generated: October 24, 2026
P-Xylene → 2-[4-(Acetyloxy)-3-fluorophenyl]-7-vinyl-1,3-benzoxazol-5-yl acetate
https://huagongshe.com/en/reaction/1007349
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Xylene | HCID 7809 | — |
| Reactant | Tributylvinyltin | HCID 81998 | — |
| Reactant | 4-[5-(Acetyloxy)-7-bromo-1,3-benzoxazol-2-yl]-2-fluorophenyl acetate | HCID 21907371 | — |
| Catalyst | HCID 178424406 | HCID 178424406 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-[4-(Acetyloxy)-3-fluorophenyl]-7-vinyl-1,3-benzoxazol-5-yl acetate | HCID 11268263 | 56.9% |
Reaction Steps
Dichlorobis(tri-o-tolylphosphine)palladium (II) (46 mg, 0.06 mmol) was added into a mixture 4-[5-(acetyloxy)-7-bromo-1,3-benzoxazol-2-yl]-2-fluorophenyl acetate (0.8 g, 1.98 mmol), tributyl(vinyl)tin (0.9 g, 2.8 mmol) and p-xylene (9 mL). The reaction mixture was stirred at 130° C. for 5 h, cooled to room temperature, diluted with ethyl ether (10 mL) and treated with activated carbon. The mixture was filtered through MgSO4 and concentrated. Purification by flash chromatography (hexanes/EtOAc 5/1) gave a white solid (0.4 g, 56% yield, m.p. 154-156° C.); MS m/e 356 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06794403B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-31dde9e36f2b42d48edde1d231e076db |
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| Source note | uspto-grants-2004_09 |
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