Hydrochloric Acid → 4-(3-Hydroxypropyl)benzene-1,3-diol

HRID 131157

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HRID 131157 반응식
[OH:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8](=[O:12])[O:9]2)=[CH:4][CH:3]=1.[BH4-].[Li+].[Cl-].[NH4+].Cl>C1COCC1.CO>[OH:12][CH2:8][CH2:7][CH2:6][C:5]1[CH:4]=[CH:3][C:2]([OH:1])=[CH:11][C:10]=1[OH:9]

참가 물질

7

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온도
65 °C

실험 절차

To a stirred solution of 7-hydroxycoumarin (7.0 g, 43.2 mmol ) in anhydrous THF (200 mL ) at rt under argon was added Lithium borohydride (2M, 65.8 mL, 129.6 mmol, 3.0 eq) solution in THF dropwise. Anhydrous methanol (1.0 mL) was added as catalyst to the reaction mixture. The mixture was heated at 65° C. for 17 h. The reaction mixture was then cooled to ambient temperature. Saturated ammonium chloride solution (40 mL) was added dropwise to the solution, followed by 1N HCl solution (40 mL). The mixture was extracted with ethyl acetate (2×100 mL). The combined organic extracts were dried (Na2SO4), filtered, and evaporated in vacuo. The residue was purified on silica gel (flash column chromatography) eluting with 30% ethyl acetate-hexane to provide the desired product as white solid (3.05 g, 42%). 1H-NMR (CD3CN) δ 6.91 (d, 1H), 6.29 (s, 1H), 6.28 (d, 1H), 3.51 (t, 2H), 2.56 (t, 2H), 1.73 (m, 2H). MS GC-MS (M+=168).

후처리

  1. temperatureThe reaction mixture was then cooled to ambient temperature
  2. extractionThe mixture was extracted with ethyl acetate (2×100 mL)
  3. dry with materialThe combined organic extracts were dried (Na2SO4)
  4. filtrationfiltered
  5. customevaporated in vacuo
  6. customThe residue was purified on silica gel (flash column chromatography)
  7. washeluting with 30% ethyl acetate-hexane

출처 및 근거

ORD 기록
ord-2fc1d2009a2d44c289d36fbe7124f4df
출처 데이터셋
uspto-grants-2008_06
특허 번호
US07384947B2

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