Methanol → 2,2-Dimethyl-4-((phenylmethoxy)methyl)-1,3-dioxolane

HRID 72073

反応式

HRID 72073 の反応式
[CH3:1][C:2]1([CH3:9])[O:6][CH:5]([CH2:7][OH:8])[CH2:4][O:3]1.CO.C[O-].[Na+].[CH2:15](Cl)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>C1(C)C=CC=CC=1>[CH2:15]([O:8][CH2:7][CH:5]1[CH2:4][O:3][C:2]([CH3:9])([CH3:1])[O:6]1)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

参加物

6

反応条件

温度
80 °C

実験手順

To a 1000 ml round-bottom flask fitted with a thermometer, a nitrogen-introducing tube, and a stirrer were added 132.2 g (1.0 mol) of 2,2-dimethyl-1,3-dioxolane-4-methanol, 202.5 g (1.05 mol) of a 28% methanol solution of sodium methoxide, and 600 ml of toluene. With introducing nitrogen thereinto, the toluene was refluxed under reduced pressure for 1 hour to remove the methanol by distillation. With maintaining the solution at 80° C., 126.6 g (1.0 mol) of benzyl chloride was added dropwise over a period of 2 hours using a dropping funnel, followed by further 2 hours of reaction. After completion of the reaction, the temperature was lowered to 60° C. and 10 g of KYOWAAD 600 was added thereto, followed by 1 hour of stirring. The reaction liquid was filtrated, the solvent was removed, and the residue was purified by distillation (b.p. 93-95° C./266 Pa) to obtain 4-(benzyloxymethyl)-2,2-dimethyl-1,3-dioxolane.

後処理

  1. customTo a 1000 ml round-bottom flask fitted with a thermometer
  2. additiona nitrogen-introducing tube, and a stirrer
  3. customto remove the methanol
  4. distillationby distillation
  5. customfollowed by further 2 hours of reaction
  6. customAfter completion of the reaction
  7. customwas lowered to 60° C.
  8. addition10 g of KYOWAAD 600 was added
  9. customThe reaction liquid
  10. filtrationwas filtrated
  11. customthe solvent was removed
  12. distillationthe residue was purified by distillation (b.p. 93-95° C./266 Pa)

出典と根拠

ORDレコード
ord-04875b4527034c489320265dac7e0f76
出典データセット
uspto-grants-2014_09
特許番号
US08828373B2

関連ノート

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