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Diethyl octylmalonate → 2-Octylpropane-1,3-diol

HRID 2050135
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HRID 2050135 반응식
C([O:3][C:4](=O)[CH:5]([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[C:6](OCC)=[O:7])C>Cl>[CH2:11]([CH:5]([CH2:4][OH:3])[CH2:6][OH:7])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 252340Diethyl octylmalonate

생성물 1

HCID 3160622-Octylpropane-1,3-diol수율 41%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

Borane methyl sulfide (BMS) complex (80 g, 1 m) was added dropwise to a mixture of diethyl-n-octylmalonate (90 g, 0.33) and tolune (400 ml) with stirring at room temperature. Stirring was continued for an additional hour. The mixture was refluxed gently for 10 hours, cooled to 20° C., and then poured slowly into ice-cold methanol (400 ml) with stirring and left to stand overnight. The solvent was stripped off and the residue was stirred with 10% hydrochloric acid solution (400 ml) overnight. The resulting mixture was extracted with chloroform (2×70 ml) and washed with water until neutral to litmus. The solvent was evaporated and the residue was vacuum distilled to yield 2-n-octylpropane-1,3-diol (25.5 g, 41%) bp 135°-140° C./0.5-0.8 mm.

후처리

  • stirringStirring
  • waitwas continued for an additional hour
  • temperatureThe mixture was refluxed gently for 10 hours
  • temperaturecooled to 20° C.
  • stirringwith stirring
  • waitleft
  • extractionThe resulting mixture was extracted with chloroform (2×70 ml)
  • washwashed with water until neutral to litmus
  • customThe solvent was evaporated
  • distillationdistilled
  • 출처 및 근거

    ORD 기록
    ord-164aeeb371254c0ab6bf951732053e6a
    출처 데이터셋
    uspto-grants-1980_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04200580

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