Monobenzone → p-Benzyloxy-(1-methylheptyloxy)benzene

HRID 579914

反応式

HRID 579914 の反応式
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+].C1(C)C=CC(S(O[CH:28]([CH3:35])[CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH3:34])(=O)=O)=CC=1.CCCCCC[C@@H](O)C>C(O)C>[CH2:1]([O:8][C:9]1[CH:10]=[CH:11][C:12]([O:15][CH:28]([CH3:35])[CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH3:34])=[CH:13][CH:14]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

6

反応物 4

HCID 7638MonobenzoneHCID 14798Sodium HydroxideHCID 2723888(+)-2-OctanolHCID 3912199p-Toluenesulfonic acid 1-methylheptyl ester

生成物 1

HCID 13878908p-Benzyloxy-(1-methylheptyloxy)benzene

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

p-Benzyloxyphenol (50 g), ethanol (150 ml) and 50% NaOH aqueous solution (25 g) were mixed with stirring, followed by pouring in the mixture, optically active 1-methylheptyl p-toluenesulfonate derived from S-(+)-2-octanol, heating the mixture under reflux for 4 hours, distilling off most of ethanol, extracting with toluene, washing with acid, alkali and water, drying, concentrating and purifying the concentrate according to column chromatography with activated alumina (150 g) to obtain oily p-benzyloxy-(1-methylheptyloxy)benzene (68.6 g), which was then subjected to hydrogenolysis with 5% Pd-C catalyst in ethanol, followed by removing the catalyst, concentrating the solution and subjecting the concentrate to vacuum distillation to obtain oily p-(1-methylheptyloxy)phenol (IIIa-2) (30.7 g) having a b.p. of 129°-130.5° C./0.5 Torr.

後処理

  1. temperatureheating the mixture
  2. temperatureunder reflux for 4 hours
  3. distillationdistilling off most of ethanol
  4. extractionextracting with toluene
  5. washwashing with acid
  6. dry with materialalkali and water, drying
  7. concentrationconcentrating
  8. custompurifying the concentrate

出典と根拠

ORDレコード
ord-9b2d367a034e4347893a65e31c228f54
出典データセット
uspto-grants-1988_06
特許番号
US04751019

関連ノート

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