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N-[(5-Chloro-2-isopropylphenyl)methylene]cyclopropanamine → N-(5-chloro-2-isopropylbenzyl)cyclopropanamine

HRID 59590
ノート
印刷プレビュー

反応式

HRID 59590 の反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH:13]([CH3:15])[CH3:14])=[C:6]([CH:8]=[N:9][CH:10]2[CH2:12][CH2:11]2)[CH:7]=1>[Pt].CO>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH:13]([CH3:15])[CH3:14])=[C:6]([CH:7]=1)[CH2:8][NH:9][CH:10]1[CH2:12][CH2:11]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 1

HCID 89875637N-[(5-Chloro-2-isopropylphenyl)methylene]cyclopropanamine

生成物 1

HCID 66158544N-(5-chloro-2-isopropylbenzyl)cyclopropanamine収率 94.6%

試薬・触媒・溶媒 2

HCID 23939Platinum触媒HCID 887Methanol溶媒

実験手順

Platinum on activated carbon (5 g, 5% Pt, dry) was added to a solution of N-[(5-chloro-2-isopropylphenyl)methylene]cyclopropanamine (III) (160.8 g, 0.725 mol) in methanol (1350 ml). The reaction vessel was subsequently flushed with nitrogen and pressurized with 6 bar of hydrogen at a maximum of 25° C. for 8 hours. The contents of the autoclave were filtered through Celite, washed with methanol and the solvent was distilled off under reduced pressure. N-(5-Chloro-2-isopropylbenzyl)cyclopropanamine of the formula (I) (153.5 g, 97.1 GC-% by area, 91.9% of theory) was obtained as a light-yellow oil.

後処理

  1. customThe reaction vessel was subsequently flushed with nitrogen
  2. filtrationThe contents of the autoclave were filtered through Celite
  3. washwashed with methanol
  4. distillationthe solvent was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-f0b7fa8a83fc42299a480f6248aca433
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09440908B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート