Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-XyleneHCID 7809—
ReactantTributylvinyltinHCID 81998—
Reactant4-[5-(Acetyloxy)-7-bromo-1,3-benzoxazol-2-yl]-2-fluorophenyl acetateHCID 21907371—
CatalystHCID 178424406HCID 178424406—
SolventDiethyl EtherHCID 3283—
Product2-[4-(Acetyloxy)-3-fluorophenyl]-7-vinyl-1,3-benzoxazol-5-yl acetateHCID 1126826356.9%

Reaction Conditions

Temperature130 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794403B2
Source datasetuspto-grants-2004_09
ORD IDord-31dde9e36f2b42d48edde1d231e076db
Source noteuspto-grants-2004_09