Chloromethyl Methyl Ether → 2-Fluoro-3-((4-propylcyclohexyl)phenyl)-1-methoxymethoxybenzene
반응식
[H-].[Na+].[F:3][C:4]1[C:9]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[CH:16]2[CH2:21][CH2:20][CH:19]([CH2:22][CH2:23][CH3:24])[CH2:18][CH2:17]2)=[CH:8][CH:7]=[CH:6][C:5]=1[OH:25].[CH3:26][O:27][CH2:28]Cl>C1COCC1.O>[F:3][C:4]1[C:9]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[CH:16]2[CH2:17][CH2:18][CH:19]([CH2:22][CH2:23][CH3:24])[CH2:20][CH2:21]2)=[CH:8][CH:7]=[CH:6][C:5]=1[O:25][CH2:26][O:27][CH3:28]참가 물질
실험 절차
Under a nitrogen atmosphere, 1.52 g of sodium hydride was added to 9.45 g of 2-fluoro-3-((4-propylcyclohexyl)phenyl)phenol (5) dissolved in 60 mL of THF cooling with iced water, and the mixture was stirred at ambient temperature for 30 minutes. 3.07 g of chloromethyl methyl ether was added to the solution under cooling with iced water, followed by stirring at ambient temperature for 4 hours. After terminating the reaction by pouring water into the reaction solution, the aqueous layer was extracted with toluene, which was added to the organic layer, and the organic layer was washed with a saturated salt solution and then dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 11.6 g of 2-fluoro-3-((4-propylcyclohexyl)phenyl)-1-methoxymethoxybenzene (6).
후처리
- stirringby stirring at ambient temperature for 4 hours
- customAfter terminating
- customthe reaction
- extractionthe aqueous layer was extracted with toluene, which
- additionwas added to the organic layer
- washthe organic layer was washed with a saturated salt solution
- dry with materialdried over anhydrous magnesium sulfate
- distillationThe solvent was distilled off
출처 및 근거
- ORD 기록
- ord-b88aec028ab3465a9637eaaccef53927
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07740769B2
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