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Water → (2-Aminomethyl-4-trifluoromethyl-phenyl)-cyclopropylmethyl-propyl-amine

HRID 604086
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HRID 604086 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH:7]1([CH2:10][N:11]([CH2:25][CH2:26][CH3:27])[C:12]2[CH:20]=[CH:19][C:18]([C:21]([F:24])([F:23])[F:22])=[CH:17][C:13]=2[CH:14]=[N:15]O)[CH2:9][CH2:8]1.O.[OH-].[Na+]>O1CCCC1>[NH2:15][CH2:14][C:13]1[CH:17]=[C:18]([C:21]([F:23])([F:24])[F:22])[CH:19]=[CH:20][C:12]=1[N:11]([CH2:10][CH:7]1[CH2:9][CH2:8]1)[CH2:25][CH2:26][CH3:27]
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참가 물질

6

반응물 4

HCID 962Water2회HCID 14798Sodium HydroxideHCID 21226445Aluminium lithium hydrideHCID 866268392-(Cyclopropylmethyl-propyl-amino)-5-trifluoromethyl-benzaldehyde oxime

생성물 1

HCID 43587121(2-Aminomethyl-4-trifluoromethyl-phenyl)-cyclopropylmethyl-propyl-amine

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매
2회

실험 절차

Lithium aluminum hydride (1.4 g) is suspended in tetrahydrofuran (50 ml) and thereto is added dropwise a 2-(cyclopropylmethyl-propyl-amino)-5-trifluoromethyl-benzaldehyde oxime (5.7 g) in tetrahydrofuran (20 ml) under ice-cooling, and the mixture is stirred at room temperature overnight. To the reaction solution are added water (1.4 ml), a 2N-aqueous sodium hydroxide solution (2.8 ml) and water (2.8 ml) successively under ice-cooling, and the insoluble material is removed by filtration and the filtrate is concentrated under reduced pressure. The resulting residue is purified by NH-silica gel column chromatography (chloroform:ethyl acetate=10:1) to give (2-aminomethyl-4-trifluoromethyl-phenyl)-cyclopropylmethyl-propyl-amine as a crude product (5.1 g).

후처리

  1. temperaturecooling
  2. customthe insoluble material is removed by filtration
  3. concentrationthe filtrate is concentrated under reduced pressure
  4. customThe resulting residue is purified by NH-silica gel column chromatography (chloroform:ethyl acetate=10:1)

출처 및 근거

ORD 기록
ord-4e33afa813bf404bba56c4b12bc2ec30
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07906517B2

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