Chloromethyl Methyl Ether → 2-Fluoro-3-((4-propylcyclohexyl)phenyl)-1-methoxymethoxybenzene
反応式
[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]参加物
実験手順
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).
後処理
- 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
出典と根拠
- ORDレコード
- ord-b88aec028ab3465a9637eaaccef53927
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07740769B2
反応ノート
読み込み中…