Potassium Iodide → N-(2,6-dimethylphenyl)-1-propyl-4-piperidinamine

HRID 1706741ノート

反応式

HRID 1706741 の反応式
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[NH:9][CH:10]1[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]1.C(=O)([O-])[O-].[Na+].[Na+].[I-].[K+].I[CH2:25][CH2:26][CH3:27]>O.C1C=CC=CC=1>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[NH:9][CH:10]1[CH2:15][CH2:14][N:13]([CH2:25][CH2:26][CH3:27])[CH2:12][CH2:11]1

参加物

7

反応物 4

HCID 4875Potassium IodideHCID 10340Sodium CarbonateHCID 336431-IodopropaneHCID 23339004N-(2,6-Dimethylphenyl)piperidin-4-amine

生成物 1

HCID 23339025N-(2,6-dimethylphenyl)-1-propyl-4-piperidinamine

試薬・触媒・溶媒 2

HCID 241Benzene溶媒2 回HCID 962Water溶媒

反応条件

温度
40 °C

実験手順

To a warm (about 40° C.) and stirred mixture of 5 parts of N-(2,6-dimethylphenyl)-4-piperidinamine, 5 parts of sodium carbonate, a few crystals of potassium iodide in 120 parts of benzene is added dropwise a solution of 5.1 parts of 1-iodopropane in 80 parts of benzene. After the addition is complete, stirring is continued for 40 hours at reflux temperature. The reaction mixture is cooled and 50 parts of water are added. The organic layer is separated, dried and evaporated in vacuo. The oily residue is distilled, yielding 10.2 parts of N-(2,6-dimethylphenyl)-1-propyl-4-piperidinamine; bp. 135° C. at 0.2 mm. pressure.

後処理

  1. additionAfter the addition
  2. stirringstirring
  3. temperatureat reflux temperature
  4. temperatureThe reaction mixture is cooled
  5. customThe organic layer is separated
  6. customdried
  7. customevaporated in vacuo
  8. distillationThe oily residue is distilled

出典と根拠

ORDレコード
ord-cc1d049652544b2db51d40cfbacfa45a
出典データセット
uspto-grants-1980_06
特許番号
US04208418

反応ノート

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