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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 660생성일: 2026년 10월 23일

Benzene, 1-bromo-3-(trifluoromethyl)- → [3-(Trifluoromethyl)phenyl](3-methoxyphenyl)amine

https://huagongshe.com/ko/reaction/660

반응식

참여 물질

역할이름HCID투입량
반응물Benzene, 1-bromo-3-(trifluoromethyl)-HCID 9817—
반응물3-MethoxyanilineHCID 10824—
시약Sodium t-butoxideHCID 23676156—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Palladium (II) acetateHCID 4144353—
용매AnisoleHCID 7519—
생성물[3-(Trifluoromethyl)phenyl](3-methoxyphenyl)amineHCID 825370280%

반응 조건

온도50 °C

반응 단계

PdOAc2 (8 mg, 0.04 mmol) and (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (40 mg, 0.07 mmol) were added to a dried vial. The vial was caped with a septa-cap and inerted with nitrogen. Degassed anisole (2 mL)was added and the catalyst mixture was heated to 50ºC for 30 minutes, then cooled down to rt. A dry 2ml microwave vial was charged with sodium 2-methylpropan-2-olate (52 mg, 0.54 mmol). It was caped and inerted with nitrogen. A degassed mixture of 1-bromo-3-(trifluoromethyl)benzene (50 µL, 0.36 mmol) and 3-methoxyaniline (50 µL, 0.45 mmol) in anisole (2 mL) wad added at rt. The catalyst solution was added to the reaction mixture. The nitrogen inlet was removed and the vial was inserted into an alumina block at 100°C. The reaction was stirred over night. After 19h, the reaction was cooled down and filtered through celite. The filtrate was concentrated. Large amounts of anisole was present. No product was detected by LCMS. The sample was descarded.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-09a52aa0a68e4624905d84eed602571e
출처 메모750 AstraZeneca ELN dataset