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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419946Generated: October 31, 2026

Toluene → 4-allyl-2-fluoroanisole

https://huagongshe.com/reaction/1419946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant4-Bromo-2-fluoroanisoleHCID 75378—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
Product4-allyl-2-fluoroanisoleHCID 275900452%

Reaction Steps

4-Bromo-2-fluoroanisole (3 g, 14.6 mmol) was dissolved in toluene (100 ml) and treated successively with tetrakis-(triphenylphosphin)-palladium (0.84 g, 0.73 mmol) and allytributylstannane (5.8 ml, 19 mmol). Reaction mixture was refluxed for 23 hours. After evaporation of the solvent, the residue was dissolved in ether (150 ml) and stirred in the presence of sat. KF (20 ml) at room temperature for 0.5 hour. Solid was filtered and H2O (100 ml) was added to the filtrate. The aqueous phase was extracted with ether (2×100 ml), combined organic phases were dried over Na2SO4 and concentrated. The residue was chromatographed over silica gel (hexan-ethyl acetate 19:1) to provide 4-allyl-2-fluoro-1-methoxy-benzene (1.26 g, 52%) as a colorless oil MS: m/e=166 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05889026
Source datasetuspto-grants-1999_03
ORD IDord-d5af5791b5aa4fb1a5943de2d1d8b520
Source noteuspto-grants-1999_03