反応式
[C:1]1([NH2:8])[CH:6]=[CH:5][C:4]([NH2:7])=[CH:3][CH:2]=1.[O:9]1[CH2:13][CH2:12][CH2:11][C:10]1=O>C([O-])(O)=O.[Na+]>[NH2:7][C:4]1[CH:5]=[CH:6][C:1]([N:8]2[CH2:13][CH2:12][CH2:11][C:10]2=[O:9])=[CH:2][CH:3]=1参加物
4
実験手順
800 mg Benzene-1,4-diamine and 600 μl Dihydro-furan-2-one were heated for 1 h to 200° C. under microwave irradiation (200 W, CEM Discover™ apparatus). Finally, 10 mL saturated NaHCO3 solution were added and the mixture was directly purified by chromatography on silica gel eluting with a gradient of DCM/MeOH 100%->50%. The fractions containing the product were combined and the solvent evaporated under reduced pressure. Yield: 860 mg.
後処理
- customthe mixture was directly purified by chromatography on silica gel eluting with a gradient of DCM/MeOH 100%->50%
- additionThe fractions containing the product
- customthe solvent evaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-4327214eb5274d1ea3ad9d089429ea25
- 出典データセット
- uspto-grants-2008_04
- 特許番号
- US07365088B2
関連ノート
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