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HRID 25027作成日:2026年10月27日

Chlorotrimethylsilane → N-(2,6-Dimethylbenzyl)phthalimide

https://huagongshe.com/reaction/25027

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物(2,6-Dimethylphenyl)methanolHCID 186748—
反応物Phthalimide potassium saltHCID 24194345—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物N-(2,6-Dimethylbenzyl)phthalimideHCID 10825581—

反応手順

To a stirred solution of 2,6-Dimethylbenzyl Alcohol (Step A, 6.59 g, 48.4 mmol) in DMSO (20 ml) was added chlorotrimethylsilane (15.75 ml, 145 mmol) at room temperature, and the mixture was stirred for one hr. To this reaction mixture were added ethyl acetate and water, the organic layer was washed with brine, dried over Na2SO4, filtered and concentrated to give an oil. The oily residue was redissolved in DMF (100 ml) and potassium phthalimide (10.76 g, 58.1 mmol) was added. The reaction mixture was stirred for 16 hours at room temperature, ethyl acetate was added, and the organic layer was washed with 3% Na2CO3, 1 N HCl, dried over Na2SO4, filtered and concentrated to give white solid. The purification was done by flash chromatography on silica gel column (chloroform:methanol 95:5) to provide the title compound as white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858602B2
出典データセットuspto-grants-2005_02
ORD IDord-b39a908e70c044be99ef9823cba1f34d
出典メモuspto-grants-2005_02