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Ethyl Acetate → [(2-Fluorophenyl)hydrazono]malonic acid

HRID 1875472
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HRID 1875472 반응식
O.[C:2]([O-:9])(=[O:8])[C:3]([C:5]([O-:7])=[O:6])=O.[Na+].[Na+].Cl.[F:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[NH:20][NH2:21].C(OCC)(=O)C>Cl.O>[F:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[NH:20][N:21]=[C:3]([C:5]([OH:7])=[O:6])[C:2]([OH:9])=[O:8]
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참가 물질

6

반응물 3

HCID 8857Ethyl AcetateHCID 2723910Hydrazine, (2-fluorophenyl)-, hydrochloride (1:1)HCID 71317420Mesoxalicacidmonohydratedisodiumsalt

생성물 1

HCID 21813250[(2-Fluorophenyl)hydrazono]malonic acid

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 962Water용매

실험 절차

Sodium mesoxalate monohydrate (2.21 g, 12.3 mmol) was dissolved in 1 M hydrochloric acid (50 ml) to give a colourless cloudy solution. 2-Fluoro-phenylhydrazine hydrochloride (2.00 g, 12.3 mmol) was added portionwise at room temperature to the stirred mixture. A yellow precipitate formed, the mixture was diluted with water (50 ml) and stirring continued overnight. Ethyl acetate (150 ml) was added, the phases were mixed vigorously until the solids had dissolved. The phases were separated and the aqueous phase was washed with ethyl acetate (50 ml). The combined organic phases were dried over magnesium sulfate, filtered and the solvent removed under vacuum. The title compound was isolated as a yellow powder (2.55 g, 11.7 mmol, 92%). LCMS: m/z 227 [M−H]+.

후처리

  1. customto give a colourless cloudy solution
  2. customA yellow precipitate formed
  3. additionthe phases were mixed vigorously until the solids
  4. dissolutionhad dissolved
  5. customThe phases were separated
  6. washthe aqueous phase was washed with ethyl acetate (50 ml)
  7. dry with materialThe combined organic phases were dried over magnesium sulfate
  8. filtrationfiltered
  9. customthe solvent removed under vacuum

출처 및 근거

ORD 기록
ord-5d83111cba0a4d8191472c4da1a9ee66
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08309552B2

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