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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808211Generated: October 30, 2026

Tributylvinyltin → Ethyl 4-fluoro-3-vinylbenzoate

https://huagongshe.com/reaction/1808211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
ReactantPotassium FluorideHCID 522689—
ReactantEthyl 3-bromo-4-fluorobenzoateHCID 24770261—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 4-fluoro-3-vinylbenzoateHCID 4694136387%

Reaction Steps

A mixture of compound ethyl 3-bromo-4-fluorobenzoate (Preparation 53, 81 g, 328.8 mmol, 1 eq) and bis(triphenylphosphine)palladium (II) chloride (7 g, 9.9 mmol, 0.03 eq) in dioxane (600 mL) was charged with nitrogen. Tin vinyltributyl (115 g, 361.6 mmol, 1.10 eq) was added and the mixture was heated to reflux overnight. The mixture was filtrated and the filtrate was concentrated in vacuum. The residue was dissolved in ether (2 L) and water (1 L). Then potassium fluoride (10 g, 1.7 mol, 5.17 eq) was added to the mixture and much of solid precipitated. The mixture was filtrated and the filtrate was separated. The aqueous phase was extracted with ether (200 mL×2). The combined organic phases were washed with brine, dried over sodium sulfate and concentrated in vacuo to give a residue. The residue was purified by chromatography (petroleum ether) to title compound as a colorless oil (55.8 g, 286 mmol, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357711B2
Source datasetuspto-grants-2013_01
ORD IDord-efcf117a2b7449049912b332ae2ec50c
Source noteuspto-grants-2013_01