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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1839582생성일: 2026년 10월 27일

Sodium Hydroxide → 4-(3-Trifluoromethyl-phenyl)-1H-indole

https://huagongshe.com/reaction/1839582

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물4-BromoindoleHCID 676494—
반응물3-(Trifluoromethyl)phenylboronic acidHCID 2734388—
촉매PalladiumHCID 23938—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4-(3-Trifluoromethyl-phenyl)-1H-indoleHCID 2256167489%

반응 조건

온도75 °C

반응 단계

To a mixture of 4-bromoindole (3.00 g, 15.3 mmol), and 3-trifluoromethylphenylboronic acid (2.91 g, 15.3 mmol) in THF (52 mL)) were added Palladium catalyst Pd(PPh3)4 (530 mg, 0.46 mmol) and the freshly prepared sodium hydroxide solution (1.84 g, 45.9 mmol in 21 mL water). The system was degassed and then charged with nitrogen. The degas procedure was repeated for three times. The mixture was stirred under nitrogen at 75° C. oil bath for 16 hours. TLC showed the completion of the coupling reaction. The mixture was cooled to room temperature, diluted with ethyl acetate, and separated from water layer. The ethyl acetate solution was washed by brine, dried over Na2SO4, and concentrated. The crude product was purified by a silica gel column eluting with hexanes—EtOAc (9:1) to provide 3.55 g (89%) of the product 4-(3-trifluoromethyl-phenyl)-1H-indole.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06677368B2
출처 데이터셋uspto-grants-2004_01
ORD IDord-ad3676c0b69b4faf930dd3717c099044
출처 메모uspto-grants-2004_01