Diethyl Ether → HCID 20028720, 화합물

HRID 1722367노트

반응식

HRID 1722367 반응식
ClC1(Cl)C(=O)[CH2:8][CH:7]2[CH:3]1[CH2:4][CH2:5][CH:6]2[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][O:16][Si](C(C)(C)C)(C)C.CC[O:27][CH2:28][CH3:29]>C(O)(=O)C.[Zn]>[OH:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][C:6]12[CH2:29][C:28](=[O:27])[CH2:8][CH:7]1[CH2:3][CH2:4][CH2:5]2

참가 물질

5

반응 조건

온도
70 °C

실험 절차

The starting material, 6,6-dichloro-2-(5-[(1,1-dimethylethyl)dimethylsiloxy]pent-1-yl)bicyclo[3.3.0]octan-7-one {1,1-dichloro-4-[5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]pentyl]hexahydro-2(1H)-pentalenone} (12.1 g, 0.30 moles) is dissolved in glacial acetic acid (85 ml) and the solution is stirred while zinc (25 g) is slowly added. The reaction is heated at 70° C. for 1 hour, after which time ether (100 ml) is added and the solution filtered. The filtrate is washed with brine and then neutralized with saturated sodium bicarbonate. The ether layer is separated and dried over anhydrous sodium sulfate. The solvent is removed under vacuum leaving a clear yellow oil. The crude product is chromatographed on silica gel and subsequently kugelrohred under vacuum leaving a clear, colorless oil (0.72 g, 3.4 mmoles).

후처리

  1. additionis slowly added
  2. filtrationthe solution filtered
  3. washThe filtrate is washed with brine
  4. customThe ether layer is separated
  5. dry with materialdried over anhydrous sodium sulfate
  6. customThe solvent is removed under vacuum
  7. customleaving a clear yellow oil
  8. customThe crude product is chromatographed on silica gel

출처 및 근거

ORD 기록
ord-07de6f9d07274b2d8da701a3827ee4ce
출처 데이터셋
uspto-grants-1989_08
특허 번호
US04855322

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