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3-Fluoro-5-[4-(methylsulfanyl)oxan-4-yl]phenol → HCID 18920179, 화합물

HRID 1291056
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HRID 1291056 반응식
[OH:1][C:2]1[CH:3]=[C:4]([C:9]2([S:15][CH3:16])[CH2:14][CH2:13][O:12][CH2:11][CH2:10]2)[CH:5]=[C:6]([F:8])[CH:7]=1.C[OH:18].O>>[OH:1][C:2]1[CH:3]=[C:4]([C:9]2([S:15]([CH3:16])=[O:18])[CH2:14][CH2:13][O:12][CH2:11][CH2:10]2)[CH:5]=[C:6]([F:8])[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 189202153-Fluoro-5-[4-(methylsulfanyl)oxan-4-yl]phenolHCID 22242641Methanol--water (1/1)

생성물 1

HCID 18920179HCID 18920179, 화합물수율 94%

실험 절차

To a stirred solution of 4-(3-hydroxy-5-fluorophenyl)-4-methylthio-3,4,5,6-tetrahydro-2H-pyran (749 mg, 3.1 mmol)(EP 462830 A2 (1991)) in methanol-water (1:1.v/v; 20 ml) cooled to 0° C. was added NalO4 (710 mg, 3.3 mmol), the ice bath removed and the mixture stirred at room temperature for 2 hours. The reaction mixture was poured into water (50 ml) and extracted with ethyl acetate (50 ml). The organic extract was washed with water (50 ml), brine (50 ml), dried (MgSO4) and concentrated in vacuo. The residual solids were purified by column chromatography on silica gel (SiO2, 150 g; ethyl acetate) to afford 752 mg (94%) of the titled compound as white solids.

후처리

  1. additionwas added NalO4 (710 mg, 3.3 mmol)
  2. custom
the ice bath removed
  • additionThe reaction mixture was poured into water (50 ml)
  • extractionextracted with ethyl acetate (50 ml)
  • extractionThe organic extract
  • washwas washed with water (50 ml), brine (50 ml)
  • dry with materialdried (MgSO4)
  • concentrationconcentrated in vacuo
  • customThe residual solids were purified by column chromatography on silica gel (SiO2, 150 g; ethyl acetate)
  • 출처 및 근거

    ORD 기록
    ord-d3ac465263f5420f9aef6b690d14c25f
    출처 데이터셋
    uspto-grants-1998_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05753682

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