Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 244403Erstellt: 25. Oktober 2026

Triethylamine → ((E)-2-phenyl-1-trifluoromethylvinyl)amine

https://huagongshe.com/reaction/244403

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktSodium HydroxideHCID 14798—
Edukt1,1,1-Trifluoro-3-phenyl-2-propanoneHCID 222958—
EduktSodium borohydrideHCID 4311764—
Edukt1-(4-Fluorophenyl)-1h-indazol-5-amineHCID 59235727—
KatalysatorTitanium TetrachlorideHCID 24193—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
Produkt((E)-2-phenyl-1-trifluoromethylvinyl)amineHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658637B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-09aaf42162be40c78eb3df57b20ac493
Quellennotizuspto-grants-2014_02