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HRID 21006作成日:2026年10月24日

Dimethylformamide → 4-Chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone

https://huagongshe.com/ja/reaction/21006

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物N,N,N',N'-TetramethylethylenediamineHCID 8037—
反応物3-chloro-N-(1-methyl-1-phenylethyl)benzamideHCID 47444761—
反応物HCID 178444656HCID 178444656—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物4-Chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinoneHCID 6849004389%

反応手順

3-Chloro-N-(1-methyl-1-phenylethyl)benzamide (7.00 g, 25.6 mmol) was dissolved in THF (280 mL), and the solution was added with TMEDA (12.4 mL, 81.9 mmol), then added with sec-butyllithium-hexane solution (0.99 mol/L, 82.7 mL, 81.9 mmol) by drops at −78° C. for 40 minutes under argon atmosphere, followed by stirring at the same temperature for 2.5 hours. Then, the mixture was added with DMF (4.36 mL, 56.3 mmol) and warmed from −78° C. to room temperature over 2 hours. The reaction mixture was added with water, 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 and the residue was purified by slurry using diisopropyl ether to obtain 4-chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone (6.86 g, yield 89%).

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-f45e4ddcaba84c37bb2475ecd5f8e92f
出典メモuspto-grants-2010_06