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2-Ethoxalylmethylcarbonylquinoline → 1-(Quinolin-2-yl)ethan-1-one

HRID 52543
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인쇄 미리보기

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HRID 52543 반응식
C([CH2:8][C:9]([C:11]1[CH:20]=[CH:19][C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[N:12]=1)=[O:10])(C(OCC)=O)=O>Cl>[C:9]([C:11]1[CH:20]=[CH:19][C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[N:12]=1)(=[O:10])[CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 199632362-Ethoxalylmethylcarbonylquinoline

생성물 1

HCID 3187031-(Quinolin-2-yl)ethan-1-one수율 96.1%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

A solution of 2-ethoxalylmethylcarbonylquinoline (32.24 g, 0.132 mol) in concentrated hydrochloric acid (300 mL) was refluxed for 4 h and concentrated in vacuo. The residue was dissolved in aqueous sodium bicarbonate and extracted with ethyl acetate. The extract was washed with water and brine, dried over magnesium sulfate, and concentrated. The residue was purified by silica gel column chromatography with 20:1 to 7:1 hexane/ethyl acetate to give 21.72 g of 2-acetylquinoline (96%): 1H NMR (270 MHz, CDCl3) δ8.25 (d, 1H, J=8.6 Hz), 8.19 (dd, 1H, J=8.3, 1 Hz), 8.13 (d, 1H, J=8.6 Hz), 7.86 (dd, 1H, J=8.3, 1 Hz), 7.78 (td, 1H, J=8.3, 1 Hz), 7.64 (td, 1H, J=8.3, 1 Hz), 2.87 (s, 3H).

후처리

  1. concentrationconcentrated in vacuo
  2. dissolutionThe residue was dissolved in aqueous sodium bicarbonate
  3. extractionextracted with ethyl acetate
  4. washThe extract was washed with water and brine
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated
  7. customThe residue was purified by silica gel column chromatography with 20:1 to 7:1 hexane/ethyl acetate

출처 및 근거

ORD 기록
ord-d2d9c123015b44638b752ce959daefa7
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05616586

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