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Ammonia → 3,4-Dimethylaniline

HRID 1414434
ノート
印刷プレビュー

反応式

HRID 1414434 の反応式
[C:1]1([CH3:12])[C:2]([CH3:11])=[CH:3][C:4](S([O-])(=O)=O)=[CH:5][CH:6]=1.[Na+].[NH2-:14].[Na+].N>>[NH2:14][C:4]1[CH:5]=[CH:6][C:1]([CH3:12])=[C:2]([CH3:11])[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 222AmmoniaHCID 24533Sodium amideHCID 23668192Sodium Xylenesulfonate

生成物 1

HCID 72483,4-Dimethylaniline収率 88.1%

実験手順

In a 200-ml autoclave were placed 35 grams (0.163 moles) of anhydrous sodium 4-o-xylene sulfonate, 14 grams (0.35 mole) of sodium amide and 120 ml of liquid ammonia in the same manner as in Example 1. The resultant mixture was heated at 120° to 125° C for 15 hours. The reaction pressure in the autoclave was 90 to 100 atm. during the reaction. After the ammonia was removed, 15 ml of methanol was added to the reaction mixture for solvolysis. Thereafter 500 ml of water was added to the product and the mixture was treated in the same manner as in Example 1, whereby 17.4 grams of 3,4-xylidine boiling at 112° C/22 mm Hg was obtained. Yield was 88.1%.

後処理

  1. customThe reaction pressure in the autoclave
  2. customduring the reaction
  3. customAfter the ammonia was removed
  4. addition15 ml of methanol was added to the reaction mixture for solvolysis
  5. additionThereafter 500 ml of water was added to the product
  6. additionthe mixture was treated in the same manner as in Example 1

出典と根拠

ORDレコード
ord-f8f117ef79994f029d7bd52f4f3a31d8
出典データセット
uspto-grants-1977_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04001313

反応ノート

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