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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 17937536, 화합물 → HCID 69588140, 화합물

HRID 1791120
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HRID 1791120 반응식
[C:1]([C:4](=[CH:9][C:10]1[CH:15]=[CH:14][C:13]([F:16])=[CH:12][C:11]=1[Cl:17])[C:5]([O:7][CH3:8])=[O:6])(=[O:3])[CH3:2].[Cl-].[CH2:19]=[N+:20]1[CH2:24][CH2:23][S:22][CH2:21]1>C(#N)C>[Cl:17][C:11]1[CH:12]=[C:13]([F:16])[CH:14]=[CH:15][C:10]=1[CH:9]=[C:4]([C:1](=[O:3])[CH2:2][CH2:19][N:20]1[CH2:24][CH2:23][S:22][CH2:21]1)[C:5]([O:7][CH3:8])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 17937536HCID 17937536, 화합물HCID 57252060Methyl 2-[(2-chloro-4-fluorophenyl)methylene]-3-oxobutanoate

생성물 1

HCID 69588140HCID 69588140, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

3.24 g (12.6 mmol) of methyl 2-acetyl-3-(2-chloro-4-fluorophenyl)acrylate from Example VII are stirred with 1.74 g (12.6 mmol) of 3-methylene-1,3-thiazolidin-3-ium chloride [prepared in analogy to H. Mohrle et al., Z. Naturforsch. 42, 1035–1046 (1987)] in 50 ml of acetonitrile at 40° C. for 48 hours. After concentration, the residue is taken up in ethyl acetate and washed with water. The organic phase is dried over sodium sulfate and concentrated, and the residue is chromatographed on silica gel with cyclohexane/ethyl acetate (5:1→2:1) as mobile phase.

후처리

  1. concentrationAfter concentration
  2. washwashed with water
  3. dry with materialThe organic phase is dried over sodium sulfate
  4. concentrationconcentrated
  5. customthe residue is chromatographed on silica gel with cyclohexane/ethyl acetate (5:1→2:1) as mobile phase

출처 및 근거

ORD 기록
ord-0778915747554df0b33f837117a41077
출처 데이터셋
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07074784B2

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