Dimethylformamide → 2-Propynyl 4-(2-propynyloxy)-3,5-dimethoxybenzoate
反応式
CN(C=O)C.[OH:6][C:7]1[C:15]([O:16][CH3:17])=[CH:14][C:10]([C:11]([OH:13])=[O:12])=[CH:9][C:8]=1[O:18][CH3:19].[CH2:20](Br)[C:21]#[CH:22].[C:24](=O)([O-])[O-].[K+].[K+].C(O[CH2:34][CH3:35])(=O)C>>[CH2:20]([O:6][C:7]1[C:8]([O:18][CH3:19])=[CH:9][C:10]([C:11]([O:13][CH2:24][C:34]#[CH:35])=[O:12])=[CH:14][C:15]=1[O:16][CH3:17])[C:21]#[CH:22]参加物
実験手順
To 100 ml of DMF were added 11.8 g of 4-hydroxy-3,5-dimethoxybenzoic acid, 15.7 g of propargyl bromide and 18 g of potassium carbonate, and the resulting mixture was stirred at room temperature for 8 hours and, then, at 80° C. for 4 hours. Thereafter, ethyl acetate was added to the reaction mixture which had been allowed to cool to near room temperature, and this was filtered through Celite (registered trade mark). To the filtrate were added successively water and dilute hydrochloric acid, followed by extraction with ethyl acetate. The organic layer was dried over magnesium sulfate, and concentrated under reduced pressure. The resulting crystals were washed with a mixed solvent of hexane and MTBE, and 15.5 g of 2-propynyl 4-(2-propynyloxy)-3,5-dimethoxybenzoate was obtained.
後処理
- waitat 80° C. for 4 hours
- temperatureto cool to near room temperature
- filtrationthis was filtered through Celite (registered trade mark)
- additionTo the filtrate were added successively water and dilute hydrochloric acid
- extractionfollowed by extraction with ethyl acetate
- dry with materialThe organic layer was dried over magnesium sulfate
- concentrationconcentrated under reduced pressure
- washThe resulting crystals were washed with a mixed solvent of hexane and MTBE
出典と根拠
- ORDレコード
- ord-c6a2c1633dd84fa5aca8ea9a77dc8865
- 出典データセット
- uspto-grants-2011_08
- 特許番号
- US08003699B2
反応ノート
読み込み中…