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Ammonia → 2,6-Dimethylcyclohexylamine

HRID 2296503
ノート
印刷プレビュー

反応式

HRID 2296503 の反応式
[O-2].[Pr+3].[O-2].[O-2].[Pr+3].[O-2].[Al+3].[O-2].[O-2].[Al+3].[CH3:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([CH3:18])[C:13]=1O.[NH3:20]>[Pd].[H][H]>[CH3:11][CH:12]1[CH2:17][CH2:16][CH2:15][CH:14]([CH3:18])[CH:13]1[NH2:20]
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

7

反応物 4

HCID 222AmmoniaHCID 113352,6-DimethylphenolHCID 165911Praseodymium oxideHCID 9989226Alumina

生成物 1

HCID 1109322,6-Dimethylcyclohexylamine収率 96%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒
HCID 178418361
HCID 178418361、化合物
溶媒

反応条件

温度
200 °C

実験手順

A catalyst consisting of 1.0% by weight of palladium and 0.5% by weight of praseodymium oxide, the remainder being aluminum oxide, in extrudate form is introduced into a 1 l cylindrical reaction tube and is heated to 200° C. A mixture of 60 g of 2,6-dimethylphenol and 360 g of liquid ammonia per hour is passed over this catalyst bed. At the same time, 100 liters (S.T.P.) of hydrogen are passed in co-current through the reaction tube under a pressure of 200 bar. The reaction product which leaves the tube is cooled under superatmospheric pressure and is then let down. About 62 g of crude product, which gives 60 g of pure 2,6-dimethylcyclohexylamine (corresponding to a yield of 96%) on distillation, are thereby obtained per hour.

後処理

  1. additionin extrudate form is introduced into a 1 l cylindrical reaction tube
  2. customThe reaction product which leaves the tube
  3. temperatureis cooled under superatmospheric pressure

出典と根拠

ORDレコード
ord-69e1b3a758594fbfa3369f462d571be0
出典データセット
uspto-grants-1984_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04429155

反応ノート

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