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Potassium Carbonate → HCID 21833755、化合物

HRID 1741068
ノート
印刷プレビュー

反応式

HRID 1741068 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:13])[CH2:9][C:10](=O)[CH3:11])=[CH:4][C:3]=1[CH3:14].Cl.[NH2:16]O.C(=O)([O-])[O-].[K+].[K+]>C(O)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:13][N:16]=[C:10]([CH3:11])[CH:9]=2)=[CH:4][C:3]=1[CH3:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 11430Potassium CarbonateHCID 443297Hydroxyamine hydrochlorideHCID 21833711HCID 21833711、化合物

生成物 1

HCID 21833755HCID 21833755、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A solution of 1-(4-bromo-3-methylphenyl)butane-1,3-dione (D77) (615 mg; 0.0024 ml) in ethanol (15 ml) was treated with hydroxylamine hydrochloride (170 mg; 0.0024 mol) and potassium carbonate (336 mg; 0.0024 mol), and the mixture heated at reflux for 2.5 hours, then overnight at room temperature. The solvent was evaporated under reduced pressure and the residue partitioned between water and ethyl acetate. The organic phase was dried (Na2SO4) and concentrated in vacuo to leave the crude isoxazole, which was purified by chromatography on silica gel, eluting with pentane, 60-80 petroleum-ether and ethyl acetate, to afford the title compound as a yellow crystalline material (477 mg, 78%).

後処理

  1. temperaturethe mixture heated
  2. temperatureat reflux for 2.5 hours
  3. customovernight
  4. customat room temperature
  5. customThe solvent was evaporated under reduced pressure
  6. customthe residue partitioned between water and ethyl acetate
  7. dry with materialThe organic phase was dried (Na2SO4)
  8. concentrationconcentrated in vacuo
  9. customto leave the crude isoxazole, which
  10. customwas purified by chromatography on silica gel
  11. washeluting with pentane, 60-80 petroleum-ether and ethyl acetate

出典と根拠

ORDレコード
ord-b0f5f9c7670044a79c08f8b9efe952ed
出典データセット
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05972951

反応ノート

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