HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643597Generated: October 29, 2026
1-Bromo-3,5-bis(trifluoromethyl)benzene → HCID 86632301, compound
https://huagongshe.com/reaction/643597
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-3,5-bis(trifluoromethyl)benzene | HCID 67602 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Methyl 2-acetamidoacrylate | HCID 98644 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 86632301 | HCID 86632301 | — |
Reaction Steps
Under a nitrogen atmosphere 50.0 g (171 mmol) 3,5-bis-(trifluoromethyl)-bromobenzene, 25.0 g (171 mmol) methyl 2-acetylamino-acrylate in 475 mL triethylamine and 250 mL acetonitrile were combined with 3.9 g (12.4 mmol) tri-o-tolyl-phosphane and 2.8 g (12.5 mmol) Pd(OAc)2 and stirred for 18 h at 80° C. After the reaction had ended the reaction mixture was evaporated down i. vac. to approx. 200 mL, combined with 400 mL EtOAc and 400 mL water, the precipitate was suction filtered and the phases were separated. The organic phase was dried over Na2SO4, combined with activated charcoal, filtered and evaporated to dryness. The residue was stirred with DIPE, suction filtered and dried i. vac.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700598B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-d39ecf55f16e4e64bf5eb4f56bd2ace3 |
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| Source note | uspto-grants-2010_04 |
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