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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 244403생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/244403

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium HydroxideHCID 14798—
반응물1,1,1-Trifluoro-3-phenyl-2-propanoneHCID 222958—
반응물Sodium borohydrideHCID 4311764—
반응물1-(4-Fluorophenyl)-1h-indazol-5-amineHCID 59235727—
촉매Titanium TetrachlorideHCID 24193—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물((E)-2-phenyl-1-trifluoromethylvinyl)amineHCID 131731205—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658637B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-09aaf42162be40c78eb3df57b20ac493
출처 메모uspto-grants-2014_02