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Water → 4-Methoxy-3-(methoxymethoxy)benzaldehyde

HRID 2254209
ノート
印刷プレビュー

反応式

HRID 2254209 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]=[O:10])=[CH:5][C:4]=1[OH:11].C(N(CC)C(C)C)(C)C.[CH3:21][O:22][CH2:23]Cl.O>CN(C)C=O>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]=[O:10])=[CH:5][C:4]=1[O:11][CH2:21][O:22][CH3:23]
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 962WaterHCID 7864Chloromethyl Methyl EtherHCID 12127IsovanillinHCID 81531Diisopropylethylamine

生成物 1

HCID 6401524-Methoxy-3-(methoxymethoxy)benzaldehyde収率 85%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
0 °C

実験手順

In 100 ml of dimethylformamide was dissolved 10 g of isovaniline, and 14 ml of N,N-diisopropylethylamine was added to the solution and the mixture was stirred. The liquid mixture was cooled to 0° C. and 7.2 ml of chloromethyl methyl ether was added to the mixture, and the temperature was elevated to room temperature and the mixture was stirred for 5 hours. After the reaction, a large quantity of water was added to the reaction mixture, and the mixture was extracted with diethyl ether, washed with water and dried. Removal of the solvent by distillation gave 11.0 g (yield=85%) of 4-methoxy-3-methoxymethoxybenzaldehyde in the form of a yellow oil.

後処理

  1. additionwas added to the solution
  2. customwas elevated to room temperature
  3. stirringthe mixture was stirred for 5 hours
  4. customAfter the reaction
  5. extractionthe mixture was extracted with diethyl ether
  6. washwashed with water
  7. customdried
  8. customRemoval of the solvent
  9. distillationby distillation

出典と根拠

ORDレコード
ord-3126b14c96df4c37936ec2ccc7a379a3
出典データセット
uspto-grants-1993_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05234951

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート