反応式
C([C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][CH:11]=1)[CH:7]=O)(O)=O.[N+:12]([CH2:15][CH3:16])([O-])=O.C([O-])(=O)C.[NH4+].CCCCCC.CCOC(C)=O>C(O)(=O)C>[NH2:12][CH:15]([CH2:7][C:6]1[CH:5]=[CH:4][CH:11]=[CH:10][CH:9]=1)[CH3:16]参加物
反応条件
- 温度
- 110 °C
実験手順
To a solution of 1.902 q (12.68 mmol) of 3-carboxybenzaldehyde in 10 mL of glacial acetic acid, was added 2.848 mL (2.970 g, 38.04mmol) of nitroethane and 1.080 g (13.95 mmol) of ammonium acetate. The solution was then heated with stirring under nitrogen in a 110° C. oil bath. Then, all of the solid went into solution near 60° C. and the mixture turned a deep yellow color. After 3 hours, thin layer chromatography with 3:1 hexane/EtOAc indicated that no starting material remained. The reaction mixture was cooled to room temperature, and then partitioned between water and methylene chloride, with acidification to about pH2 with 6 M HCl. The organic layer was washed with 6 M HCl, then dried with magnesium sulfate. The solvents were then removed with a rotary evaporator, yielding 2.768 g (98%) of crude material, which was carried on without further purification because of the difficulty of chromatographing the very polar carboxylic acid.
後処理
- temperatureThe solution was then heated
- customwent into solution near 60° C.
- temperatureThe reaction mixture was cooled to room temperature
- custompartitioned between water and methylene chloride, with acidification to about pH2 with 6 M HCl
- washThe organic layer was washed with 6 M HCl
- dry with materialdried with magnesium sulfate
- customThe solvents were then removed with a rotary evaporator
出典と根拠
- ORDレコード
- ord-7a70ff8e997d4bfa9b19dbd164d8ecc5
- 出典データセット
- uspto-grants-1993_11
- 特許番号
- US05262333
関連ノート
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