Sulfuric Acid → Diethyl (3-chloro-2,4-difluorobenzoyl)malonate
반응식
[Mg].[C:2]([O:10][CH2:11][CH3:12])(=[O:9])[CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5].[Cl:13][C:14]1[C:15]([F:24])=[C:16]([CH:20]=[CH:21][C:22]=1[F:23])[C:17](Cl)=[O:18].S(=O)(=O)(O)O>C(O)C.C1(C)C=CC=CC=1.C(Cl)(Cl)(Cl)Cl>[Cl:13][C:14]1[C:15]([F:24])=[C:16]([CH:20]=[CH:21][C:22]=1[F:23])[C:17]([CH:3]([C:4]([O:6][CH2:7][CH3:8])=[O:5])[C:2]([O:10][CH2:11][CH3:12])=[O:9])=[O:18]참가 물질
반응 조건
- 온도
- 60 °C
실험 절차
3.9 g (0.16 mol) of magnesium are introduced into 8.6 ml of ethanol, and the reaction is started up using carbon tetrachloride. A solution of 23.1 g (0.144 mol) of diethyl malonate in 16.3 ml of ethanol is added dropwise at an internal temperature of 50°-60° C. in such a manner that the temperature is maintained. The mixture is subsequently stirred for one hour at 60° C. A solution of 31.3 g (0.148 mol) of 3-chloro-2,4-difluorobenzoyl chloride in 16 ml of toluene is then added dropwise at -10° to -5° C., and stirring is continued for one hour at 0° C. and subsequently overnight while the mixture comes to room temperature. The reaction mixture is poured into ice-water, acidified using 10 ml of concentrated sulphuric acid and extracted using toluene. The toluene phase is washed using saturated sodium chloride solution, and the solvent is removed in vacuo.
후처리
- temperatureis maintained
- stirringstirring
- waitis continued for one hour at 0° C. and subsequently overnight while the mixture
- customcomes to room temperature
- extractionextracted
- washThe toluene phase is washed
- customthe solvent is removed in vacuo
출처 및 근거
- ORD 기록
- ord-5ed51ee65e9d41f5ad9b0827b8619d48
- 출처 데이터셋
- uspto-grants-1995_10
- 특허 번호
- US05457104
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