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HRID 21083作成日:2026年10月23日

Chloromethyl Methyl Ether → 3-methoxymethoxy-N-(1-methyl-1-phenylethyl)benzamide

https://huagongshe.com/ja/reaction/21083

反応式

関与物質

役割名称HCID仕込み量
反応物Chloromethyl Methyl EtherHCID 7864—
反応物Sodium HydroxideHCID 14798—
反応物DiisopropylethylamineHCID 81531—
反応物Hydrate;hydrochlorideHCID 21885828—
反応物3-acetoxy-N-(1-methyl-1-phenylethyl)benzamideHCID 68490335—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物3-methoxymethoxy-N-(1-methyl-1-phenylethyl)benzamideHCID 6849279584%

反応手順

3-Acetoxy-N-(1-methyl-1-phenylethyl)benzamide (9.57 g, 32.2 mmol) was dissolved in methanol (190 mL), and the solution was added with 4 mol/L sodium hydroxide solution (32.2 mL), followed by stirring at room temperature for 20 minutes. The reaction mixture was added with 1 mol/L hydrochloric acid water to adjust the pH to 7, and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was dissolved in dichloromethane (190 mL), and the solution was added with diisopropylethylamine (16.8 mL, 96.6 mmol) and chloromethyl methyl ether (3.70 mL, 48.3 mmol) under ice-cooling. Then, the reaction mixture was warmed to room temperature and stirred for 2 hours. The mixture was added with diisopropylethylamine (5.60 mL, 32.2 mmol) and chloromethyl methyl ether (1.20 mL, 15.8 mmol), followed by further stirring for 2 hours. The reaction mixture was added with water and extracted with chloroform. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography (chloroform/methanol=100/0, 99/1) to obtain 3-methoxymethoxy-N-(1-methyl-1-phenylethyl)benzamide (8.09 g, yield 84%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745641B2
出典データセットuspto-grants-2010_06
ORD IDord-ba349968fa0843f6b91c6590150476ff
出典メモuspto-grants-2010_06