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Diisopropylamine → 3-(4-Chlorophenyl)prop-2-yn-1-amine

HRID 597872
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반응식

HRID 597872 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5](I)=[CH:4][CH:3]=1.[CH2:9]([NH2:12])[C:10]#[CH:11].C(NC(C)C)(C)C>C(Cl)Cl.CCOC(C)=O.[Cu]I.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:11]#[C:10][CH2:9][NH2:12])=[CH:4][CH:3]=1
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참가 물질

8

반응물 3

HCID 7912DiisopropylamineHCID 125101-Chloro-4-iodobenzeneHCID 239041Propargylamine

생성물 1

HCID 589523443-(4-Chlorophenyl)prop-2-yn-1-amine

시약·촉매·용매 4

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매HCID 178418476
HCID 178418476, 화합물
촉매
HCID 6344Dichloromethane용매
HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 4-chloro iodobenzene (25 g) in 400 mL CH2Cl2 at room temperature was added propargyl amine (13.5 mL), diisopropyl amine (37 mL), CuI (4 g) and Pd(PPh3)2Cl2 (3.7 g). The mixture was stirred overnight at room temperature, diluted with 600 mL EtOAc and filtered through a CELITE pad to remove insoluble materials. The solution washed with water, brine, dried over MgSO4, concentrated and purified by chromatography to provide 14.1 g of 3-(4-chloro-phenyl)-prop-2-ynylamine. MS: m/e 166.1 (MH+)

후처리

  1. filtrationfiltered through a CELITE pad
  2. customto remove insoluble materials
  3. washThe solution washed with water, brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated
  6. custompurified by chromatography

출처 및 근거

ORD 기록
ord-efc44ef22a6745ec93de5fb19b92ad4c
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07897601B2

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