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2-(4-Fluorophenyl)-1-(4-(methylsulfonyl)phenyl)ethanone → HCID 9841715, 화합물

HRID 1058983
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HRID 1058983 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([C:11]2[CH:16]=[CH:15][C:14]([S:17]([CH3:20])(=[O:19])=[O:18])=[CH:13][CH:12]=2)=[O:10])=[CH:4][CH:3]=1>C(O)(=O)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[C:9](=[O:10])[CH:8]=[C:5]([CH3:4])[O:10][C:9]=2[C:11]2[CH:16]=[CH:15][C:14]([S:17]([CH3:20])(=[O:19])=[O:18])=[CH:13][CH:12]=2)=[CH:6][CH:7]=1
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참가 물질

3

반응물 1

HCID 111970952-(4-Fluorophenyl)-1-(4-(methylsulfonyl)phenyl)ethanone

생성물 1

HCID 9841715HCID 9841715, 화합물

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
140 °C

실험 절차

To a solution of 2-(4-fluorophenyl)-1-(4-methanesulfonylphenyl)ethanone (1 g; 3.4 moles) in glacial acetic acid (15 ml), polyphosphoric acid (10 g) was added and then heated at 140° C. for 16 hours. After cooling, the reaction was poured into ice-water, extracted with ethyl acetate (2×50 ml), the organic solution dried (Na2SO4) and the solvent removed under reduced pressure. The residual oil was purified by column chromatography with silica gel and ethyl acetate as eluent. 3-(4-fluorophenyl)-2-(4-methanesulfonylphenyl)-6-methylpyran-4-one was obtained (0.5 g) m.p. 237° C. (Compound 2 in Table 4).

후처리

  1. temperatureAfter cooling
  2. extractionextracted with ethyl acetate (2×50 ml)
  3. dry with materialthe organic solution dried (Na2SO4)
  4. customthe solvent removed under reduced pressure
  5. customThe residual oil was purified by column chromatography with silica gel and ethyl acetate as eluent

출처 및 근거

ORD 기록
ord-b9456205aadf42bc9d659bc8928f084f
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06518303B2

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