Hydrochloric Acid → 2-(2,3-Dimethylphenoxy)-2-methylpropanoic acid
반응식
[OH-].[Na+].[CH3:3][C:4]1[C:9]([CH3:10])=[CH:8][CH:7]=[CH:6][C:5]=1[OH:11].Br[C:13]([CH3:18])([CH3:17])[C:14]([OH:16])=[O:15].Cl>C(OCC)C.O.C(C(C)=O)C>[CH3:3][C:4]1[C:9]([CH3:10])=[CH:8][CH:7]=[CH:6][C:5]=1[O:11][C:13]([CH3:18])([CH3:17])[C:14]([OH:16])=[O:15]참가 물질
반응 조건
- 온도
- 50 °C
실험 절차
Sodium hydroxide (82.0 g, 2.05 mol) was added to a solution of methyl ethyl ketone (400 mL) containing 2,3-dimethylphenol (50.0 g, 410 mmol), and the mixture was stirred at 50° C. for 1 hour. After that, a solution of methyl ethyl ketone (200 mL) containing 2-bromo-2-methylpropionic acid (103 g, 615 mmol) was added thereto, and the mixture was stirred at 50° C. for 4 hours. After cooled to room temperature, the reaction solution was distributed by adding water and diethyl ether. 6N hydrochloric acid was added to the aqueous layer to be acidic, and then extraction was performed using ethyl acetate. The extract was washed with saturated saline, and then dried using anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the obtained residue was purified by silica gel chromatography (hexane-ethyl acetate 95:5 to 50/50) to give 38.3 g of the title compound (yield: 45%).
후처리
- additionwas added
- stirringthe mixture was stirred at 50° C. for 4 hours
- temperatureAfter cooled to room temperature
- extractionextraction
- washThe extract was washed with saturated saline
- customdried
- customThe solvent was removed under reduced pressure
- customthe obtained residue was purified by silica gel chromatography (hexane-ethyl acetate 95:5 to 50/50)
출처 및 근거
- ORD 기록
- ord-05ac9e0818184a36b03892f6a79883e2
- 출처 데이터셋
- uspto-grants-2012_10
- 특허 번호
- US08288390B2
반응 노트
불러오는 중…