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3-Aminophenol → 3-Ethoxymethoxyphenylamine

HRID 1246571
ノート
印刷プレビュー

反応式

HRID 1246571 の反応式
[H-].[Na+].[NH2:3][C:4]1[CH:5]=[C:6]([OH:10])[CH:7]=[CH:8][CH:9]=1.[CH2:11]([O:13][CH2:14]Cl)[CH3:12]>C(#N)C>[CH2:11]([O:13][CH2:14][O:10][C:6]1[CH:5]=[C:4]([NH2:3])[CH:9]=[CH:8][CH:7]=1)[CH3:12]
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

5

反応物 3

HCID 115683-AminophenolHCID 18523Chloromethyl ethyl etherHCID 24758Sodium hydride

生成物 1

HCID 120677493-Ethoxymethoxyphenylamine

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒2 回

反応条件

温度
0 °C

実験手順

12 g (274.9 mmol) of a dispersion of sodium hydride (55% in oil) was added portionwise at 0° C. to a solution of 20.0 g (183.3 mmol) of 3-aminophenol in 450 mL of dried acetonitrile. The mixture was then allowed to agitate at 0° C. for 3 hours. A solution of 25 g (210.8 mmol) of chloromethyl ethyl ether in 30 mL of acetonitrile was added dropwise, and the mixture was allowed to agitate overnight at room temperature. The reaction mixture was then filtered and the filter cake was washed with a small amount of acetone and the filtrate was evaporated. This gave 32.3 g of 3-ethoxymethoxyphenylamine. The resulting product was used in the next step without further purification.

後処理

  1. stirringto agitate overnight at room temperature
  2. filtrationThe reaction mixture was then filtered
  3. washthe filter cake was washed with a small amount of acetone
  4. customthe filtrate was evaporated
  5. customThe resulting product was used in the next step without further purification

出典と根拠

ORDレコード
ord-6ac75bfba4484f3fae43dcee6a8cae9c
出典データセット
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07128764B2

反応ノート

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