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4-Hydroxybenzaldehyde → 4-(2-Phenoxyethoxy)benzaldehyde

HRID 1739404
ノート
印刷プレビュー

反応式

HRID 1739404 の反応式
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1.[H-].[Na+].[O:12]([CH2:19][CH2:20]CS([O-])(=O)=O)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>CN(C=O)C>[O:12]([CH2:19][CH2:20][O:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1
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 1264-HydroxybenzaldehydeHCID 24758Sodium hydrideHCID 21841067HCID 21841067、化合物

生成物 1

HCID 134832164-(2-Phenoxyethoxy)benzaldehyde収率 64.4%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

1.19 g of 4-hydroxybenzaldehyde were dissolved in 30 ml of DMF, and 0.41 g of 60% NaH were further added to the resultant solution while cooling it with ice. The solution was then stirred for 1 hour after elevating the temperature of the solution up to room temperature. The solution was again cooled with ice, then added with 2.0 g of 2-phenoxyethyl-methane sulfonate, and stirred for 1 hour at room temperature and subsequently for a night at 50-60° C. The solution reacted was poured into ice-water and extracted with ethyl acetate, then the organic layer resulted was dried with anhydrous magnesium sulfate. The solvent used was then removed by distillation under reduced pressure, and the residue obtained was washed with a mixture of ether and hexane, thereby affording 1.45 g of 4-(2-phenoxyethyloxy)benzaldehyde.

後処理

  1. temperaturewhile cooling it with ice
  2. customup to room temperature
  3. temperatureThe solution was again cooled with ice
  4. stirringstirred for 1 hour at room temperature and subsequently for a night at 50-60° C
  5. customThe solution reacted
  6. extractionextracted with ethyl acetate
  7. customthe organic layer resulted
  8. dry with materialwas dried with anhydrous magnesium sulfate
  9. customThe solvent used was then removed by distillation under reduced pressure
  10. customthe residue obtained
  11. washwas washed with a mixture of ether and hexane

出典と根拠

ORDレコード
ord-2070c0609afe47438e3a39baf707cd68
出典データセット
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05965743

反応ノート

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