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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 552688생성일: 2026년 10월 25일

4-(Trifluoromethyl)phenol → Rac-[5-methanesulfonyl-2-((s)-2,2,2-trifluoro-1-methyl-ethoxy)-phenyl]-[3-(4-trifluoromethyl-phenoxymethyl)-pyrrolidin-1-yl]-methanone

https://huagongshe.com/reaction/552688

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참여 물질

역할이름HCID투입량
반응물4-(Trifluoromethyl)phenolHCID 67874—
반응물Di-tert-butyl azodicarboxylateHCID 97268—
반응물2-PyridyldiphenylphosphineHCID 621893—
반응물Rac-(3-hydroxymethyl-pyrrolidin-1-yl)-[5-methanesulfonyl-2-((s)-2,2,2-trifluoro-1-methyl-ethoxy)-phenyl]-methanoneHCID 59030469—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Rac-[5-methanesulfonyl-2-((s)-2,2,2-trifluoro-1-methyl-ethoxy)-phenyl]-[3-(4-trifluoromethyl-phenoxymethyl)-pyrrolidin-1-yl]-methanoneHCID 59030456—

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온도70 °C

반응 단계

To a solution of 70 mg rac-(3-Hydroxymethyl-pyrrolidin-1-yl)-[5-methanesulfonyl-2-((S)-2,2,2-trifluoro-1-methyl-ethoxy)-phenyl]-methanone (Example C1) in 1.4 ml tetrahydrofuran were added 30 mg 4-hydroxybenzotrifluoride and 50 mg diphenyl-2-pyridylphosphine. 43 mg Di-tert-butyl azodicarboxylate was added. The mixture was stirred at 70° C. for 23 hours. The solvent was removed in vacuo. The oil was purified on silica gel (eluent: ethyl acetate) to yield a yellow gum. The gum was dissolved in ethyl acetate. The solution was washed 3 times with HCl 5N, once with water, dried over Na2SO4, filtered and concentrated in vacuo to provide the title compound as a light yellow foam. MS (m/e): 540.3 (M+H+, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07951836B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-65eb1d6bb9254bd2b1f1f32ac9968b90
출처 메모uspto-grants-2011_05