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Tetrahydrofuran → HCID 18969768, 화합물

HRID 399073
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HRID 399073 반응식
CO[C:3]1([CH2:24]CCC)[C:6](=[O:7])[C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[C:4]1[C:14]1[CH:19]=[CH:18][C:17]([S:20]([CH3:23])(=[O:22])=[O:21])=[CH:16][CH:15]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3].[CH2:34]1COCC1>>[CH3:24][C:3]1([CH3:34])[CH:6]([OH:7])[C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[C:4]1[C:14]1[CH:15]=[CH:16][C:17]([S:20]([CH3:23])(=[O:22])=[O:21])=[CH:18][CH:19]=1
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참가 물질

4

반응물 3

HCID 8028TetrahydrofuranHCID 18969745HCID 18969745, 화합물HCID 21226445Aluminium lithium hydride

생성물 1

HCID 18969768HCID 18969768, 화합물

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온도
0 °C

실험 절차

To a solution of Example 14 (100 mg) in THF (1 mL) at 0° C., was added LAH (1M, THF, 920 μL). The mixture was stirred at 0° C. for min., quenched with H2O, and diluted with EtOAc. The organic phase was washed with HCl 1N, brine, dried (MgSO4) and the solvents evaporated. The residue was purified by flash chromatography (silica gel; hexane/EtOAc (70:30)) to give the title compound as a white solid, m.p. 79°-81° C.

후처리

  1. custom, quenched with H2O
  2. additiondiluted with EtOAc
  3. washThe organic phase was washed with HCl 1N, brine
  4. dry with materialdried (MgSO4)
  5. customthe solvents evaporated
  6. customThe residue was purified by flash chromatography (silica gel; hexane/EtOAc (70:30))

출처 및 근거

ORD 기록
ord-cb53d749ac4440cf90ed5c416bfc733e
출처 데이터셋
uspto-grants-1998_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05817700

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