HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420102Generated: October 25, 2026
Triethylamine → Ethyl (4-fluorophenyl)-[4-{isopropoxy}-3-vinylphenyl]-phosphinate
https://huagongshe.com/reaction/420102
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Bromo-1-isopropoxy-2-vinylbenzene | HCID 12542425 | — |
| Reactant | HCID 178527040 | HCID 178527040 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl (4-fluorophenyl)-[4-{isopropoxy}-3-vinylphenyl]-phosphinate | HCID 68043962 | 82% |
Reaction Steps
To a degassed mixture of 4-fluoro-phenylphosphinate (2.07 g, 11.0 mmol) and 4-bromo-1-isopropoxy-2-vinylbenzene (2.43 g, 10.0 mmol) in acetonitrile (66 mL) were added triethylamine (3.1 mL, 22.0 mmol), palladium acetate (112 mg, 0.5 mmol), and 1,1′-bis(diphenylphosphino)ferrocene (277 mg, 0.5 mmol). The mixture was heated at 68° C. for 24 hrs. The volatiles were removed in vacuo, and the residue was purified by column chromatography using 40 to 80% ethyl acetate in petroleum ether to afford 2.84 g of compound BA2 in 82% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093379B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-9d338dc698f14be18b6d658a99864929 |
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| Source note | uspto-grants-2012_01 |
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