Trifluoroacetic acid → HCID 59397871, 화합물

HRID 2193097노트

반응식

HRID 2193097 반응식
[O:1]1CCO[CH:2]1[CH2:6][N:7]1[C:16]2[C:11](=[CH:12][C:13]([CH:17]([CH3:19])[CH3:18])=[CH:14][CH:15]=2)[CH:10]=[CH:9][C:8]1=[O:20].FC(F)(F)C(O)=O>>[CH:17]([C:13]1[CH:12]=[C:11]2[C:16](=[CH:15][CH:14]=1)[N:7]([CH2:6][CH:2]=[O:1])[C:8](=[O:20])[CH:9]=[CH:10]2)([CH3:19])[CH3:18]

참가 물질

3

반응물 2

HCID 6422Trifluoroacetic acidHCID 59398048HCID 59398048, 화합물

생성물 1

HCID 59397871HCID 59397871, 화합물

실험 절차

To 0.42 g of 1-(1,3-dioxolan-2-ylmethyl)-6-isopropylquinolin-2(1H)-one, 4 mL of a 90% aqueous trifluoroacetic acid solution was added, and the mixture was stirred at room temperature overnight. The solvent was removed under reduced pressure, and ethyl acetate and an aqueous saturated sodium hydrogen carbonate solution were added thereto. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and the extract were combined, the resultant solution was washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain 0.41 g of a pale yellow oily substance, (6-isopropyl-2-oxoquinolin-1(2H)-yl)acetaldehyde.

후처리

  1. customThe solvent was removed under reduced pressure, and ethyl acetate
  2. additionan aqueous saturated sodium hydrogen carbonate solution were added
  3. customThe organic layer was separated
  4. extractionthe aqueous layer was extracted with ethyl acetate
  5. washthe resultant solution was washed with an aqueous saturated sodium chloride solution
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customthe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-aa24b59cae114fc8894888ad68d53c88
출처 데이터셋
uspto-grants-2012_12
특허 번호
US08329694B2

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