Ethyl Acetate → HCID 7172095、化合物
反応式
F[B-](F)(F)F.[O:6]=[N+:7]=[O:8].[C:9]([C:13]1[CH:14]=[CH:15][C:16]([OH:21])=[C:17]([CH:20]=1)[CH:18]=[O:19])([CH3:12])([CH3:11])[CH3:10].C(OCC)(=O)C.C([O-])(O)=O.[Na+]>C(#N)C>[C:9]([C:13]1[CH:14]=[C:15]([N+:7]([O-:8])=[O:6])[C:16]([OH:21])=[C:17]([CH:20]=1)[CH:18]=[O:19])([CH3:12])([CH3:10])[CH3:11]参加物
反応条件
- 温度
- -15 °C
実験手順
At −30° C. 4.84 g nitroniumtetrafluoroborate are added to a solution of 5.00 g 5-tert-butyl-2-hydroxy-benzaldehyde in 200 ml acetonitrile. The solution is heated to −15° C. within 1 h and then combined with ethyl acetate and saturated aqueous NaHCO3 solution. The resulting mixture is extracted with ethyl acetate, and the combined extracts are washed with saturated aqueous saline solution, dried (MgSO4) and evaporated down. The residue is taken up in 2 ml of water and 40 ml concentrated acetic acid, and the resulting mixture is refluxed for 2 h. The cooled solution is poured into ice-cold water, and the precipitate formed is filtered off and dissolved in ethyl acetate. The organic solution is dried (MgSO4) and evaporated down. The oil remaining rapidly solidifies.
後処理
- customAt −30° C
- extractionThe resulting mixture is extracted with ethyl acetate
- washthe combined extracts are washed with saturated aqueous saline solution
- dry with materialdried (MgSO4)
- customevaporated down
- temperature40 ml concentrated acetic acid, and the resulting mixture is refluxed for 2 h
- additionThe cooled solution is poured into ice-cold water
- customthe precipitate formed
- filtrationis filtered off
- dissolutiondissolved in ethyl acetate
- dry with materialThe organic solution is dried (MgSO4)
- customevaporated down
出典と根拠
- ORDレコード
- ord-7fad12f122484f8f96a1237ed039aa89
- 出典データセット
- uspto-grants-2015_02
- 特許番号
- US08946438B2
反応ノート
読み込み中…