HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1912874Erstellt: 26. Oktober 2026
4-Bromo-3-(trifluoromethyl)aniline → 3-Trifluoromethyl-4-vinylaniline
https://huagongshe.com/reaction/1912874
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Bromo-3-(trifluoromethyl)aniline | HCID 67852 | — |
| Edukt | Potassium trifluorovinylborate | HCID 86620274 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Lösungsmittel | Tert-Butylamine | HCID 6385 | — |
| Produkt | 3-Trifluoromethyl-4-vinylaniline | HCID 23155172 | 79,2% |
Reaktionsschritte
In 20 mL of isopropanol, 10 mL of water and 5 mL of t-butylamine, 4.0 g (16.7 mmol) of 4-bromo-3-(trifluoromethyl)aniline was dissolved, and 4.0 g (29.9 mmol) of potassium (trifluoro)vinylborate and 300 mg (0.37 mmol) of PdCl2(dppf)2•2(dichloromethane) complex were added thereto, and the mixture solution was stirred in an argon atmosphere at 80° C. for 20 hours. The reaction solution was concentrated and the residue was partitioned between water and ethyl acetate, and the organic layer was washed with a saturated sodium chloride solution and concentrated under reduced pressure. The product was purified by a silica gel column (n-hexane:ethyl acetate=6:1) to obtain 2.475 g (79%) of a target product as a pale yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08609656B2 |
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| Quelldatensatz | uspto-grants-2013_12 |
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| ORD ID | ord-744a22c9d51640a2a06e84a07a95c9aa |
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| Quellennotiz | uspto-grants-2013_12 |
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