Toluene → 2-(4-(4-Oxocyclohexyl)cyclohexyl)-5-n-butyl-1,3-dioxane

HRID 2119279ノート

反応式

HRID 2119279 の反応式
C1(C)C=CC=CC=1.[O:8]=[C:9]1[CH2:14][CH2:13][CH:12]([CH:15]2[CH2:20][CH2:19][CH:18]([CH:21]=[O:22])[CH2:17][CH2:16]2)[CH2:11][CH2:10]1.[CH2:23]([CH:27]([CH2:30]O)[CH2:28][OH:29])[CH2:24][CH2:25][CH3:26].C1(C)C=CC(S(O)(=O)=O)=CC=1>O>[O:8]=[C:9]1[CH2:10][CH2:11][CH:12]([CH:15]2[CH2:20][CH2:19][CH:18]([CH:21]3[O:29][CH2:28][CH:27]([CH2:23][CH2:24][CH2:25][CH3:26])[CH2:30][O:22]3)[CH2:17][CH2:16]2)[CH2:13][CH2:14]1

参加物

6

実験手順

To 300 ml of toluene were added 20.2 g (97.0 mmol) of the 4-(4-oxocyclohexyl)cyclohexanecarbaldehyde described above, 12.8 g (96.8 mmol) of 2-n-butyl-1,3-propanediol, and 1 g of p-toluenesulfonic acid, and the mixture was refluxed by using a Dean-Stark for 2 hours. Water in an amount of 200 ml was added to the reaction solution, the product thus formed was extracted with toluene, the extract was washed with saturated aqueous bicarbonate solution and water in this turn, and then the solvent was distilled off. After the residue was purified by column chromatography on silica gel (eluent: heptane/ethyl acetate=5/1), the solvent was distilled off. The residue was Silo recrystallized from ethanol to give 3.2 g (9.9 mmol) of 2-(4-(4-oxocyclohexyl)-cyclohexyl)-5-n-butyl-1,3-dioxane. Yield of this compound based on 4-(4-oxocyclohexyl)cyclohexanecarbaldehyde was 10%.

後処理

  1. temperaturethe mixture was refluxed
  2. customfor 2 hours
  3. customthe product thus formed
  4. extractionwas extracted with toluene
  5. washthe extract was washed with saturated aqueous bicarbonate solution and water in this turn
  6. distillationthe solvent was distilled off
  7. customAfter the residue was purified by column chromatography on silica gel (eluent: heptane/ethyl acetate=5/1)
  8. distillationthe solvent was distilled off
  9. customrecrystallized from ethanol

出典と根拠

ORDレコード
ord-cc35a6cc6fde456f815653fcc5ae3f0e
出典データセット
uspto-grants-2004_02
特許番号
US06685995B1

反応ノート

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