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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 379647생성일: 2026년 10월 26일

Iodine → (2R)-1-(2,5-Difluorophenyl)-2-((tetrahydro-2H-pyran-2-yl)oxy)propan-1-one

https://huagongshe.com/reaction/379647

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Ammonium ChlorideHCID 25517—
반응물2-Bromo-1,4-difluorobenzeneHCID 67862—
반응물MagnesiumHCID 5462224—
반응물(2R)-1-morpholino-2-((tetrahydro-2H-pyran-2-yl)oxy)propan-1-oneHCID 10977653—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(2R)-1-(2,5-Difluorophenyl)-2-((tetrahydro-2H-pyran-2-yl)oxy)propan-1-oneHCID 1019930698.3%

반응 조건

온도52.5 °C

반응 단계

A mixture of magnesium (7.25 g, 0.298 mol) and iodine (catalytic amount) and 1-bromo-2,5-difluorobenzene (20.0 g, 0.178 mol) in THF (250ml ) was vigously stirred. The color of iodine was disappeared and the inner temperature rose up to 65° C. To this mixture was added additional 1-bromo-2,5-difluorobenzene (30.0 g, 0.267 mol) dropwise to maintain the inner temperature from 50 to 55° C. over 45min. The resulting mixture was stirred at 55° C. for 30min. then at r.t. for 1 hr. The mixture was cooled down to −5° C. To this mixture was added a solution of 4-[(2R)-2-(3,4,5,6-Tetrahydro-2H-pyran-2-yloxy)propionyl]morpholine (52.5 g, 0.216 mol ) in THF (150ml) dropwise over 40min. And the resulting mixture was stirred at r.t. for 4hrs. The reaction mixture was cooled down to 5° C. and saturated NH4Cl aq. (100ml) was added carefully. The whole was diluted with H2O (600ml) and extracted with EtOAc (400 ml+200 ml×2). The combined organic layer was dried over Na2SO4 and concentrated in vacuo. The residue was chromatographed on silica gel (n-hexane: EtOAc=10:1˜5:1) to give (2R)-2′,5′-Difluoro-2-(3,4,5,6-tetrahydro-2H-pyran-2-yloxy)-propiophenone (47.3 g, 81% ) as pale yellow syrup.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06300353B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-66395d86b59b4abfbbf2224b95c3671c
출처 메모uspto-grants-2001_10