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3-Bromothiophene-2-carboxaldehyde → 3-(Pyridine-2-sulfonyl)thiophene-2-carbaldehyde

HRID 1944462
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인쇄 미리보기

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HRID 1944462 반응식
[Na+].[N:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8]([O-:10])=[O:9].Br[C:12]1[CH:16]=[CH:15][S:14][C:13]=1[CH:17]=[O:18]>CS(C)=O>[N:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8]([C:12]1[CH:16]=[CH:15][S:14][C:13]=1[CH:17]=[O:18])(=[O:10])=[O:9]
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참가 물질

4

반응물 2

HCID 27970793-Bromothiophene-2-carboxaldehydeHCID 23678794Sodium Pyridine-2-sulfinate

생성물 1

HCID 866521883-(Pyridine-2-sulfonyl)thiophene-2-carbaldehyde수율 6.4%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

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온도
125 °C

실험 절차

A mixture of pyridine-2-sulfinate sodium salt (8.5 g), 3-bromothiophene-2-carbaldehyde (6.5 g) and dimethyl sulfoxide (50 mL) (split equally into four microwave vials) was heated by microwave irradiation at 125° C. for 45 minutes. The combined mixtures were diluted with ethyl acetate, washed with saturated aqueous sodium hydrogen carbonate solution and saturated aqueous sodium chloride solution and dried over magnesium sulfate. The solvent was removed under reduced pressure and the residue was purified by column chromatography on silica gel, eluting with a mixture of dichloromethane and ethyl acetate (1:0 to 0:1 by volume) to afford the title compound as a yellow solid (0.55 g).

후처리

  1. customsplit equally into four microwave vials)
  2. additionThe combined mixtures were diluted with ethyl acetate
  3. washwashed with saturated aqueous sodium hydrogen carbonate solution and saturated aqueous sodium chloride solution
  4. dry with materialdried over magnesium sulfate
  5. customThe solvent was removed under reduced pressure
  6. customthe residue was purified by column chromatography on silica gel
  7. washeluting with a mixture of dichloromethane and ethyl acetate (1:0 to 0:1 by volume)

출처 및 근거

ORD 기록
ord-d9748e056adf4ca4a7766893eebf3c61
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08394836B2

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