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Ethylene Glycol → 2-(4-Nitrophenyl)-1,3-dioxolane

HRID 1039832
ノート
印刷プレビュー

反応式

HRID 1039832 の反応式
[N+:1]([C:4]1[CH:11]=[CH:10][C:7]([CH:8]=[O:9])=[CH:6][CH:5]=1)([O-:3])=[O:2].[CH2:12](O)[CH2:13][OH:14].C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([CH:8]2[O:14][CH2:13][CH2:12][O:9]2)=[CH:10][CH:11]=1)([O-:3])=[O:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 174Ethylene GlycolHCID 5414-NitrobenzaldehydeHCID 6101p-Toluenesulfonic acid

生成物 1

HCID 2667962-(4-Nitrophenyl)-1,3-dioxolane収率 92%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

A stirred solution of p-nitrobenzaldehyde (101.5 g, 672 mmol), ethylene glycol (112 mL) and p-toluenesulfonic acid (12.8 g, 67.2 mmol) in toluene (800 mL) was heated in flask equipped with a Dean-Stark trap at 120° C. for 4 h. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure. To the residue was added saturated aqueous sodium bicarbonate (800 mL) and this mixture was stirred at room temperature for 15 min. The resulting solid was isolated by filtration and dried under vacuum to give the title compound (121.8 g, 92% yield) as a yellow solid.

後処理

  1. customequipped with a Dean-Stark trap at 120° C. for 4 h
  2. concentrationthe reaction mixture was concentrated under reduced pressure
  3. additionTo the residue was added saturated aqueous sodium bicarbonate (800 mL)
  4. customThe resulting solid was isolated by filtration
  5. customdried under vacuum

出典と根拠

ORDレコード
ord-c06bb860e31e468797e1029fbed9a65b
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08551978B2

反応ノート

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