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Ethanol → 2-(6-Carbethoxyoctyl)-2-cyclopentenone

HRID 442086
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인쇄 미리보기

반응식

HRID 442086 반응식
[C:1]([CH:4]([CH2:16][CH3:17])[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]1[C:11](=[O:15])[CH2:12][CH2:13][CH:14]=1)([OH:3])=[O:2].S(Cl)(Cl)=O.[CH2:22](O)[CH3:23]>>[C:1]([CH:4]([CH2:16][CH3:17])[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]1[C:11](=[O:15])[CH2:12][CH2:13][CH:14]=1)([O:3][CH2:22][CH3:23])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702EthanolHCID 24386Thionyl ChlorideHCID 217678162-(6-Carboxyoctyl)-2-cyclopentenone

생성물 1

HCID 132897872-(6-Carbethoxyoctyl)-2-cyclopentenone

실험 절차

Treatment of 2-(6-carboxyoctyl)-2-cyclopentenone (Example 154) with thionyl chloride and then treatment of the acid chloride with ethanol in the manner described in Example 264 give an amber oil. The oil is placed on a magnesia-silica gel column and eluted with 3:1 benzene:ether. The solvent is removed and the residue is distilled, b.p. 122° C. (0.06 mm).

후처리

  1. customgive an amber oil
  2. washeluted with 3:1 benzene
  3. customThe solvent is removed
  4. distillationthe residue is distilled

출처 및 근거

ORD 기록
ord-86a3e98002304651b99d0962b4509a2a
출처 데이터셋
uspto-grants-1977_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04044043

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