Oxygen → 1-(Ethoxycarbonyloxy)ethyl 5-(2,4-difluorophenyl)salicylate
反応式
[Cl-].[Na+].C([O-])(=O)C.[Na+].C1(=O)OCCO1.[C:14]([O:23][CH:24]([O:26][C:27]([O:29][CH2:30][CH3:31])=[O:28])[CH3:25])(=[O:22])[C:15]1[C:16](=[CH:18][CH:19]=[CH:20][CH:21]=1)[OH:17].[F:32][C:33]1[CH:38]=[CH:37][CH:36]=[C:35]([F:39])[CH:34]=1.O=O.[OH-].[Na+]>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.C(O)(=O)C>[F:32][C:33]1[CH:34]=[C:35]([F:39])[CH:36]=[CH:37][C:38]=1[C:20]1[CH:21]=[C:15]([C:14]([O:23][CH:24]([O:26][C:27]([O:29][CH2:30][CH3:31])=[O:28])[CH3:25])=[O:22])[C:16]([OH:17])=[CH:18][CH:19]=1参加物
反応物 7
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 25 °C
実験手順
A glass-lined autoclave is charged with 1 mmole of palladium acetate, 5 mmole of sodium chloride, 1.6 mmole of sodium acetate, 2 mmole of phosphomolybdenovanadic acid, 10 g of ethylene carbonate, 5.0 ml of acetic acid, 465 mmole of 1-(ethoxycarbonyloxy)ethyl salicylate, and 510 mmole of m-difluorobenzene. The mixture is stirred for 48 hours at 90° C. and under 200 psi oxygen pressure. The solution is cooled to 25° C. and excess m-difluorobenzene is removed by distillation. Fifty ml of water and 150 ml of toluene are then added to the residue. The pH is adjusted to 7-8 with aqueous sodium hydroxide (80 mmoles). The layers are separated and the aqueous solution is extracted with 150 ml of toluene. The toluene and then the excess starting materials are removed by distillation. The resulting residue is recrystallized from methanol to obtain pure 1-(ethoxycarbonyloxy)ethyl 5-(2,4-difluorophenyl)salicylate.
後処理
- customexcess m-difluorobenzene is removed by distillation
- additionFifty ml of water and 150 ml of toluene are then added to the residue
- customThe layers are separated
- extractionthe aqueous solution is extracted with 150 ml of toluene
- customare removed by distillation
- customThe resulting residue is recrystallized from methanol
出典と根拠
- ORDレコード
- ord-ea78099213ba4e3993de00f16675cdd1
- 出典データセット
- uspto-grants-1985_09
- 特許番号
- US04542158
反応ノート
読み込み中…