HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808211Generated: October 30, 2026
Tributylvinyltin → Ethyl 4-fluoro-3-vinylbenzoate
https://huagongshe.com/reaction/1808211
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylvinyltin | HCID 81998 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Ethyl 3-bromo-4-fluorobenzoate | HCID 24770261 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl 4-fluoro-3-vinylbenzoate | HCID 46941363 | 87% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357711B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-efcf117a2b7449049912b332ae2ec50c |
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| Source note | uspto-grants-2013_01 |
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