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HRID 3697作成日:2026年10月24日

N-Trimethylsilyl-N-methylacetamide → N-(2-hydroxy-1-phenylethyl)-benzamide

https://huagongshe.com/ja/reaction/3697

反応式

関与物質

役割名称HCID仕込み量
反応物N-Trimethylsilyl-N-methylacetamideHCID 81953—
反応物Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 613145—
反応物(R)-beta-aminophenethyl alcoholHCID 2724025—
溶媒DichloromethaneHCID 6344—
生成物N-(2-hydroxy-1-phenylethyl)-benzamideHCID 14150746—

反応手順

A slurry of (R)-2-amino-2-phenylethanol (1.0 g, 7.4 mmol) in 50 mL dichloromethane was allowed to stir with N-methyl-N-(trimethylsilyl)acetamide (3.4 mL, 21.1 mmol) until a homogenous solution occured. The solution was cooled to 0° C. to 5° C. and a solution of 2,2'-dithiobis[benzoyl chloride] (1.0 g, 2.9 mmol) in 20 mL dichloromethane was added. The solution was stirred for 2 hours and 1 mL of 50% aqueous acetic was added causing the crude product to precipitate from solution. This solid was collected by filtration, washed with 1N HCl, water, and recrystallized from dimethylformamide/water to afford 1.2 g of the title compound, mp 235°-236° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05734081
出典データセットuspto-grants-1998_03
ORD IDord-45e1e2f32fac4e2c92640fb69c3a608f
出典メモuspto-grants-1998_03