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Water → 4-Cyclopropyl-6-methoxy-1,3,5-triazin-2-amine

HRID 462344
ノート
印刷プレビュー

反応式

HRID 462344 の反応式
[NH2:1][C:2]1[N:7]=[C:6]([CH:8]2[CH2:10][CH2:9]2)[N:5]=[C:4](C(Cl)(Cl)Cl)[N:3]=1.[CH3:15][O-:16].[Na+].O>CO>[NH2:1][C:2]1[N:7]=[C:6]([CH:8]2[CH2:10][CH2:9]2)[N:5]=[C:4]([O:16][CH3:15])[N: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

5

反応物 3

HCID 962WaterHCID 10942334Sodium MethoxideHCID 201996154-Cyclopropyl-6-(trichloromethyl)-1,3,5-triazin-2-amine

生成物 1

HCID 27265914-Cyclopropyl-6-methoxy-1,3,5-triazin-2-amine

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
60 °C

実験手順

25.3 g of 2-amino-4-cyclopropyl-6-trichloromethyl-1,3,5-triazine are added to a solution of 10.8 g of sodium methylate in 50 ml of methanol, and the mixture is stirred at 60° C. for 80 minutes. There are added 300 ml of water, and the formed suspension is filtered. The filter residue is suspended twice in 100 ml of acetyl acetate each time, and again filtered. The organic phases are collected, dried over magnesium sulfate and concentrated by evaporation to thus obtain an oil, which crystallises when stirred up in ether. The yield is 6.7 g of the title compound, m.p. 158°-159° C.

後処理

  1. filtrationthe formed suspension is filtered
  2. filtrationagain filtered
  3. customThe organic phases are collected
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated by evaporation
  6. customto thus obtain an oil, which
  7. customcrystallises when
  8. stirringstirred up in ether

出典と根拠

ORDレコード
ord-702aed28a5ad4b1f81db9fb2b11a1601
出典データセット
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04515626

反応ノート

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