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N-tert-butyl-1-benzhydryl-3-methylazetidin-3-amine hydrochloride → HCID 68455629、化合物

HRID 474000
ノート
印刷プレビュー

反応式

HRID 474000 の反応式
[ClH:1].[C:2]([NH:6][C:7]1([CH3:24])[CH2:10][N:9](C(C2C=CC=CC=2)C2C=CC=CC=2)[CH2:8]1)([CH3:5])([CH3:4])[CH3:3]>C(O)C.[OH-].[OH-].[Pd+2]>[ClH:1].[C:2]([NH:6][C:7]1([CH3:24])[CH2:10][NH:9][CH2:8]1)([CH3:5])([CH3:4])[CH3:3]
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

4

反応物 1

HCID 68457650N-tert-butyl-1-benzhydryl-3-methylazetidin-3-amine hydrochloride

生成物 1

HCID 68455629HCID 68455629、化合物

試薬・触媒・溶媒 2

HCID 9942167Palladium hydroxide触媒HCID 702Ethanol溶媒

反応条件

温度
40 °C

実験手順

To a slurry of N-tert-butyl-1-benzhydryl-3-methylazetidin-3-amine hydrochloride (1.69 g, 4.91 mmol) in ethanol (30 ml) was added 10% Palladium hydroxide on carbon (160 mg) and the mixture degassed three times with nitrogen and three times with hydrogen. The mixture was then stirred under a hydrogen atmosphere 40° C. (warm water bath) for 3 h and then at room temperature for a further 12 h. The reaction was degassed with nitrogen and filtered through celite and concentrated. The compound was used crude in subsequent chemistry. 1H NMR (MeOH) 1.50 (9H, s), 1.99 (3H, s), 4.19 (2H, d), 4.91 (2H, d).

後処理

  1. customthe mixture degassed three times with nitrogen and three times with hydrogen
  2. temperature(warm water bath) for 3 h
  3. customThe reaction was degassed with nitrogen
  4. filtrationfiltered through celite
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-0782814961ff4b6a99953b6ac4568a52
出典データセット
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08637511B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート