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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1023643생성일: 2026년 10월 24일

N,N'-Dimethylethylenediamine → 10-[(R)-4-(2,2,2-trifluoro-1-hydroxy-ethyl)-phenyl]-1,4-dioxa-10-aza-dispiro[4.2.4.2]tetradecan-9-one

https://huagongshe.com/ko/reaction/1023643

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참여 물질

역할이름HCID투입량
반응물N,N'-DimethylethylenediamineHCID 8070—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물1,4-Dioxa-10-azadispiro[4.2.4.2]tetradecan-9-oneHCID 58230108—
반응물2,2,2-Trifluoro-1-(4-iodophenyl)ethanolHCID 59440865—
반응물(R)-2,2,2-trifluoro-1-(4-iodophenyl)ethanolHCID 68227618—
용매DimethylformamideHCID 6228—
생성물10-[(R)-4-(2,2,2-trifluoro-1-hydroxy-ethyl)-phenyl]-1,4-dioxa-10-aza-dispiro[4.2.4.2]tetradecan-9-oneHCID 5823010364.6%

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온도80 °C

반응 단계

1,4-Dioxa-10-aza-dispiro[4.2.4.2]tetradecan-9-one (352 mg, obtained in example 133, step 3) was dissolved in DMF (22 mL) at RT. Then, (R)-2,2,2-trifluoro-1-(4-iodophenyl)ethanol (755 mg, for synthesis see: J. Org. Chem. 2009, 74, 1605-1610), N,N′-dimethylethylenediamine (sym) (294 mg), cuprous iodide (476 mg) and K3PO4 (1.06 g) were added to the reaction mixture. The mixture was heated to 80° C. for 4.5 hours. The reaction mixture was cooled down to 30° C. and more 2,2,2-trifluoro-1-(4-iodophenyl)ethanol (252 mg) was added. The mixture was re-heated to 80° C. for 2 hours. The reaction mixture was cooled, poured into ice/water and extracted two times with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, filtered and the solvent was evaporated. The residue was purified by flash chromatography (silica gel, gradient of ethyl acetate in heptane) to give the title compound as a colorless solid (415 mg, 62%). MS (ESI): 386.4 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08722721B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-e4dede784b1d45d1add7db7199971c82
출처 메모uspto-grants-2014_05