HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 244403Erstellt: 25. Oktober 2026
Triethylamine → ((E)-2-phenyl-1-trifluoromethylvinyl)amine
https://huagongshe.com/reaction/244403
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 1,1,1-Trifluoro-3-phenyl-2-propanone | HCID 222958 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 1-(4-Fluorophenyl)-1h-indazol-5-amine | HCID 59235727 | — |
| Katalysator | Titanium Tetrachloride | HCID 24193 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | ((E)-2-phenyl-1-trifluoromethylvinyl)amine | HCID 131731205 | — |
Reaktionsschritte
To a solution of 100 mg (0.44 mmol) of 1-(4-fluorophenyl)-1H-indazol-5-ylamine in 5 mL of dichloromethane was added 60 μL (1.04 mmol) of 1,1,1-trifluoro-3-phenylpropan-2-one, 70 μL (0.97 mmol) of triethylamine followed by 130 μL (1.02 mmol) of TiCl4. The mixture was stirred for 20 hours and then MeOH was added followed by 200 mg (5.29 mmol) of sodium borohydride. After 1 hour, the mixture was diluted 50 mL of 1N aqueous NaOH and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate, and concentrated in vacuo. The crude material was purified by Combiflash chromatography using a EtOAc-hexanes (0-70% gradient) to provide 70 mg (37%) of [144-fluorophenyl)-1H-indazol-5-yl]-((E)-2-phenyl-1-trifluoromethylvinyl)amine as a yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08658637B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-09aaf42162be40c78eb3df57b20ac493 |
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| Quellennotiz | uspto-grants-2014_02 |
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