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

HRID 2214968
ノート
印刷プレビュー

反応式

HRID 2214968 の反応式
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1.[I-].[K+].CC(C)([O-])C.[K+].[CH3:18][O:19][CH2:20][CH2:21]Cl>CN(C=O)C>[CH3:18][O:19][CH2:20][CH2:21][O:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 1264-HydroxybenzaldehydeHCID 4875Potassium IodideHCID 123162-Chloroethyl methyl etherHCID 23665647Potassium tert-butoxide

生成物 1

HCID 64855604-(2-Methoxyethoxy)benzaldehyde

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
80 °C

実験手順

146.5 g (1.2 mol) of 4-hydroxybenzaldehyde are dissolved in DMF, and 20 g (0.12 mol) of potassium iodide, 134.6 g (1.2 mol) of potassium tert-butoxide and 170.2 g (1.8 mol) of 2-chloroethyl methyl ether are added. The reaction mixture is stirred at 80° C. for 16 h. For work-up, the reaction mixture is concentrated under reduced pressure. The residue is taken up in 1 l of ethyl acetate and extracted with 0.5 l of 1N aqueous sodium hydroxide solution. The ethyl acetate phase is dried using magnesium sulphate and concentrated under reduced pressure. The residue obtained after concentration is distilled under high vacuum (b.p.=100° C. at 0.45 mbar). This gives 184.2 g (85% of theory) of product.

後処理

  1. concentrationFor work-up, the reaction mixture is concentrated under reduced pressure
  2. extractionextracted with 0.5 l of 1N aqueous sodium hydroxide solution
  3. dry with materialThe ethyl acetate phase is dried
  4. concentrationconcentrated under reduced pressure
  5. customThe residue obtained
  6. concentrationafter concentration
  7. distillationis distilled under high vacuum (b.p.=100° C. at 0.45 mbar)

出典と根拠

ORDレコード
ord-ceca3998d8a546c1a9ad185bb0a38d12
出典データセット
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07109218B2

反応ノート

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