HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675458Generated: October 26, 2026
Triethylamine → Ethyl [4-(trifluoromethyl)phenyl]-{4-(isopropoxy)-3-vinylphenyl}phosphinate
https://huagongshe.com/reaction/1675458
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Bromo-1-isopropoxy-2-vinylbenzene | HCID 12542425 | — |
| Reactant | HCID 178476782 | HCID 178476782 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl [4-(trifluoromethyl)phenyl]-{4-(isopropoxy)-3-vinylphenyl}phosphinate | HCID 66650623 | 8.6% |
Reaction Steps
To a degassed solution of ethyl 4-(trifluoromethyl)-phenylphosphinate (1.00 g, 4.20 mmol) and 4-bromo-1-isopropoxy-2-vinylbenzene (921 mg, 3.81 mmol) in DMF (40 mL) were added the triethylamine (1.1 mL, 7.62 mmol) and tris(dibenzylideneacetone)dipalladium (698 mg, 0.762 mmol). The mixture was warmed at 70° C. overnight. The volatiles were removed in vacuo and the residue was purified by column chromatography using 5 to 100% ethyl acetate in petroleum ether to afford compound BA1 (130 mg) as a dark green oil in 8.6% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08003659B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-d818e4fcb11f46dcb9290acd5cc35fb9 |
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| Source note | uspto-grants-2011_08 |
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