Benzylamine → 1-Benzyl-4-tert-butyl-piperazine

HRID 1657753

反応式

HRID 1657753 の反応式
Cl[CH2:2][CH2:3][N:4]([CH2:9][CH2:10]Cl)[C:5]([CH3:8])([CH3:7])[CH3:6].[CH2:12]([NH2:19])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>C(O)C>[CH2:12]([N:19]1[CH2:10][CH2:9][N:4]([C:5]([CH3:8])([CH3:7])[CH3:6])[CH2:3][CH2:2]1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

参加物

4

反応物 2

HCID 7504BenzylamineHCID 96167Triethylamine, 2',2''-dichloro-1,1-dimethyl-

生成物 1

HCID 35919371-Benzyl-4-tert-butyl-piperazine

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒3 回

実験手順

A solution of 2000 g of bis-(2-chloroethyl)-tert-butylamine in 500 cc of ethanol and a solution of 1095 g of benzylamine in 750 cc of ethanol are simultaneously added dropwise to 1000 cc of boiling ethanol. After the addition is complete, the reaction mixture is heated to the boil for 1 hour. The mixture is subsequently concentrated in a vacuum and the residue is dissolved in dilute hydrochloric acid. The acid solution is washed with ether and is subsequently rendered alkaline with a concentrated, aqueous sodium hydroxide solution. The liberated base is extracted with ether and the ether residue is distilled. 1-benzyl-4-tert-butyl piperazine has a B.P. of 160°-162° at 12 mm of Hg.

後処理

  1. additionAfter the addition
  2. temperaturethe reaction mixture is heated to the boil for 1 hour
  3. concentrationThe mixture is subsequently concentrated in a vacuum
  4. dissolutionthe residue is dissolved in dilute hydrochloric acid
  5. washThe acid solution is washed with ether
  6. extractionThe liberated base is extracted with ether
  7. distillationthe ether residue is distilled

出典と根拠

ORDレコード
ord-b0a805842af4428eaa3f82b69830ea24
出典データセット
uspto-grants-1976_06
特許番号
US03962248

関連ノート

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