戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1766013作成日:2026年10月27日

Triethylamine → 2-[3-(4-chlorophenyl)propyl]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/1766013

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Sodium HydroxideHCID 14798—
反応物Methanesulfonyl chlorideHCID 31297—
反応物4-ChlorobenzenepropanolHCID 221971—
反応物Phthalimide potassium saltHCID 24194345—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物2-[3-(4-chlorophenyl)propyl]-1H-isoindole-1,3(2H)-dioneHCID 1784890792.3%

反応手順

Mesyl chloride (2.10 ml, 27.1 mmol) was added to a solution of 3-(4-chlorophenyl)propyl alcohol (4.6 g, 27 mmol) obtained in 1) above and triethylamine (3.78 ml, 27.1 mmol) in tetrahydrofuran (100 ml) at 0° C. and stirred at room temperature for 30 minutes. Water was added to the reaction mixture which was then extracted with ethyl acetate. The extract was washed with an aqueous saturated NaCl solution and dried over anhydrous magnesium sulfate. After the solvent was distilled away under reduced pressure, the reaction mixture and potassium phthalimide (5.02 g, 27.1 mmol) were dissolved in dimethylformamide and heated at 80° C. for 10 hours under stirring. 8 N aqueous sodium hydroxide was added to the resultant solution which was then extracted with ethyl acetate. The extract was washed with an aqueous saturated NaCl solution and dried over anhydrous magnesium sulfate. The solvent was distilled away under reduced pressure, whereby 7.47 g 2-[3-(4-chlorophenyl)propyl]-1H-isoindole-1,3(2H)-dione was obtained as solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07229986B2
出典データセットuspto-grants-2007_06
ORD IDord-ad7a9c8a03a7489e8fad45aebf568bb8
出典メモuspto-grants-2007_06