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

HRID 1944462
ノート
印刷プレビュー

反応式

HRID 1944462 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

HCID 866521883-(Pyridine-2-sulfonyl)thiophene-2-carbaldehyde収率 6.4%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

反応条件

温度
125 °C

実験手順

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).

後処理

  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)

出典と根拠

ORDレコード
ord-d9748e056adf4ca4a7766893eebf3c61
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08394836B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート