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Water → Methyl 1-(2-methylquinolin-8-yl)cyclopropanecarboxylate

HRID 338908
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HRID 338908 반응식
[CH3:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[C:5]([CH2:12][C:13]([O:15][CH3:16])=[O:14])[CH:6]=[CH:7][CH:8]=2)[N:3]=1.[H-].[Na+].Br[CH2:20][CH2:21]Cl.O>CS(C)=O.C1COCC1.CCOCC>[CH3:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[C:5]([C:12]3([C:13]([O:15][CH3:16])=[O:14])[CH2:21][CH2:20]3)[CH:6]=[CH:7][CH:8]=2)[N:3]=1
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참가 물질

8

반응물 4

HCID 962WaterHCID 78491-Bromo-2-ChloroethaneHCID 24758Sodium hydrideHCID 70984092Methyl 2-(2-methylquinolin-8-yl)acetate

생성물 1

HCID 70984245Methyl 1-(2-methylquinolin-8-yl)cyclopropanecarboxylate수율 47.6%

시약·촉매·용매 3

HCID 679Dimethyl Sulfoxide
용매
HCID 3283Diethyl Ether용매
HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of methyl 2-(2-methylquinolin-8-yl)acetate (0.78 g, 3.62 mmol) in DMSO (10 mL) and THF (5 mL) was added 60% NaH (0.72 g, 18.12 mmol) and the reaction mixture was stirred at ambient temperature for 30 minutes. 1-Bromo-2-chloroethane (0.90 mL, 10.87 mmol) was added slowly, and the reaction mixture was stirred at ambient temperature for 40 hours. Water (10 mL) and ether (50 mL) were added. The organic layer was separated, washed with brine, dried (sodium sulfate), filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (7:1 hexane/ethyl acetate) to give methyl 1-(2-methylquinolin-8-yl)cyclopropanecarboxylate (0.416 g, 47.6%) as an oil.

후처리

  1. stirringthe reaction mixture was stirred at ambient temperature for 40 hours
  2. customThe organic layer was separated
  3. washwashed with brine
  4. dry with materialdried (sodium sulfate)
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by flash chromatography on silica gel (7:1 hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-d3057b49f7e0408a974652012d4c042f
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08889704B2

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