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Sodium Cyanide → 2-Oxo-1,2,3,4-tetrahydroquinoline-5-carbonitrile

HRID 1521650
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HRID 1521650 반응식
Cl[C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][C:6](=[O:12])[NH:7]2.[C-:13]#[N:14].[Na+]>CN1CCCC1=O.O.[Ni](Br)Br>[O:12]=[C:6]1[CH2:5][CH2:4][C:3]2[C:2]([C:13]#[N:14])=[CH:11][CH:10]=[CH:9][C:8]=2[NH:7]1
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참가 물질

6

반응물 2

HCID 8929Sodium CyanideHCID 190277365-chloro-3,4-dihydroquinolin-2(1H)-one

생성물 1

HCID 665969262-Oxo-1,2,3,4-tetrahydroquinoline-5-carbonitrile

시약·촉매·용매 3

HCID 278492Nickel(II) bromide촉매HCID 962Water용매HCID 13387N-methyl-2-pyrrolidone용매

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온도
200 °C

실험 절차

To a stirred solution of 5-chloro-3,4-dihydroquinolin-2(1H)-one (143-4; 1.8 g, 0.0099 mol) and nickel bromide (2.15 g, 0.0099 mol) in N-methyl-2-pyrrolidone (10 mL) was added sodium cyanide (0.97 g, 0.0198 mol) portion wise at room temperature. Reaction mixture was heated at 200° C. for 10 min under microwave irradiation. The reaction mixture was diluted with water (50 mL) and extracted with ethyl acetate (2×100 mL). The combined organic layer was washed with saturated aqueous sodium chloride solution, dried over sodium sulphate and concentrated under vacuum to obtain the title compound. MS (M−1): 171.2.

후처리

  1. customReaction mixture
  2. extractionextracted with ethyl acetate (2×100 mL)
  3. washThe combined organic layer was washed with saturated aqueous sodium chloride solution
  4. dry with materialdried over sodium sulphate
  5. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-3d4428a24cfa436f8d6162aacafb0694
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09073929B2

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