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

HRID 2050135
ノート
印刷プレビュー

反応式

HRID 2050135 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 252340Diethyl octylmalonate

生成物 1

HCID 3160622-Octylpropane-1,3-diol収率 41%

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

実験手順

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.

後処理

  • 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
  • 出典と根拠

    ORDレコード
    ord-164aeeb371254c0ab6bf951732053e6a
    出典データセット
    uspto-grants-1980_04
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04200580

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