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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 226539생성일: 2026년 10월 25일

Benzenamine, 3,5-bis(trifluoromethyl)- → 2-[5-(3,5-Bis-trifluoromethyl-phenylamino)-4'-chloro-3'-trifluoromethyl-biphenyl-3-yl]-4-methyl-pentanoic acid methyl ester

https://huagongshe.com/reaction/226539

반응식

참여 물질

역할이름HCID투입량
반응물Benzenamine, 3,5-bis(trifluoromethyl)-HCID 9480—
반응물(1,1'-Binaphthalen)-2-yldi-tert-butylphosphineHCID 2734941—
반응물Sodium t-butoxideHCID 23676156—
반응물2-(4'-Chloro-5-trifluoromethanesulfonyloxy-3'-trifluoromethyl-biphenyl-3-yl)-4-methyl-pentanoic acid methyl esterHCID 57754964—
촉매palladium(II) acetateHCID 167845—
용매TolueneHCID 1140—
생성물2-[5-(3,5-Bis-trifluoromethyl-phenylamino)-4'-chloro-3'-trifluoromethyl-biphenyl-3-yl]-4-methyl-pentanoic acid methyl esterHCID 5775505645.8%

반응 단계

A mixture of 2-(4′-chloro-5-trifluoromethanesulfonyloxy-3′-trifluoromethyl-biphenyl-3-yl)-4-methyl-pentanoic acid methyl ester (48 mg, 0.10 mmol), 3,5-bis-(trifluoromethyl)-aniline (18 μL, 0.12 mmol), sodium tert-butoxide (9.8 mg, 0.10 mmol), Pd(OAc)2 (2.5 mg, 0.01 mmol), 2-(di-tert-butylphoshino-1,1′-binaphthyl (3.5 mg, 0.01 mmol) and toluene (1 mL) was stirred under microwave irradiation at 130° C. for 3×10 min. The mixture was diluted with toluene (9 mL), washed with 1M HCl (2×10 mL) and brine (10 mL), dried (MgSO4), concentrated in vacuo and purified by flash column chromatography (diethylether-petroleum ether) to afford the title product as a colourless powder (28 mg, 44%). Mass spectrum (ESI, m/z): 610, 612 (M−H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557244B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-f17439eb2c694957a946408cc6238aa7
출처 메모uspto-grants-2009_07