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2,4-Difluorobenzaldehyde → HCID 54311230, 화합물

HRID 1976579
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HRID 1976579 반응식
[C:1]([CH2:5][C:6]([O:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:7])(=[O:4])[CH2:2][CH3:3].[F:16][C:17]1[CH:24]=[C:23]([F:25])[CH:22]=[CH:21][C:18]=1[CH:19]=O>C1C=CC=CC=1.C([O-])(=O)C.[NH2+]1CCCCC1>[F:16][C:17]1[CH:24]=[C:23]([F:25])[CH:22]=[CH:21][C:18]=1[CH:19]=[C:5]([C:1](=[O:4])[CH2:2][CH3:3])[C:6]([O:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 737702,4-DifluorobenzaldehydeHCID 12425357HCID 12425357, 화합물

생성물 1

HCID 54311230HCID 54311230, 화합물수율 100.3%

시약·촉매·용매 2

HCID 3014295Piperidinium acetate촉매HCID 241Benzene용매

실험 절차

A solution of benzyl propionylacetate (157 g, 0.758 mol), 2,4-difluorobenzaldehyde (107.65 g, 0.758 mol), and piperidinium acetate (5.49 g, 38 mmol) in benzene (1 L) were stirred at room temperature for 96 h. The mixture was washed with water (2×100 mL), dried (magnesium sulfate) and the solvent evaporated under reduced pressure to yield the product as a pale yellow syrup (251.2 g) which was used in the next step without further purification.

후처리

  1. washThe mixture was washed with water (2×100 mL)
  2. dry with materialdried (magnesium sulfate)
  3. customthe solvent evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-d780222aeaf04921bd40715d72f6d110
출처 데이터셋
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06228861B1

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