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

HRID 59590
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HRID 59590 반응식
[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
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참가 물질

4

반응물 1

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

생성물 1

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

시약·촉매·용매 2

HCID 23939Platinum촉매HCID 887Methanol용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-f0b7fa8a83fc42299a480f6248aca433
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09440908B2

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