反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:8]([OH:13])=[CH:9][C:10]=1[O:11][CH3:12])[CH:6]=[O:7].C(=O)([O-])[O-].[K+].[K+].[CH3:20][N:21]([CH3:26])[S:22](Cl)(=[O:24])=[O:23].O>CN(C=O)C>[CH3:20][N:21]([CH3:26])[S:22](=[O:24])(=[O:23])[O:13][C:8]1[CH:9]=[C:10]([O:11][CH3:12])[C:3]([O:2][CH3:1])=[CH:4][C:5]=1[CH:6]=[O:7]参加物
6
反応条件
- 温度
- 10 °C
実験手順
Dissolve 16.2 g (0.0889 mol) of 3,4-dimethoxy-6-hydroxybenzaldehyde in 80 ml of DMF. Cool to 10° C. and add in portions 24.6 g (0.178 mol) of potassium carbonate. Allow to return to ambient temperature and stir for 30 minutes. Cool to approximately 10° C. and pour in dropwise 10.1 ml (0.093 mol) of N,N-dimethylsulphamoyl chloride. Allow to return to ambient temperature and stir for 2 h. Pour the reaction mixture into 600 g of water and ice and stir for 1 h at ambient temperature. The precipitate formed is filtered off and washed 3 times with 50 ml of water each time and then dried in vacuo. 21.3 g of title product are obtained.
後処理
- customto return to ambient temperature
- temperatureCool to approximately 10° C.
- customto return to ambient temperature
- stirringstir for 2 h
- stirringstir for 1 h at ambient temperature
- customThe precipitate formed
- filtrationis filtered off
- washwashed 3 times with 50 ml of water each time
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-c010bd7aa97d4a2297e58994385f2b9a
- 出典データセット
- uspto-grants-2012_01
- 特許番号
- US08097720B2
関連ノート
読み込み中…