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HRID 1356707作成日:2026年10月27日

Acetic Anhydride → Amides, C5-9, N-(3-(dimethylamino)propyl)

https://huagongshe.com/reaction/1356707

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物N,N-Dimethyl-1,3-propanediamineHCID 7993—
反応物Sodium HydroxideHCID 14798—
溶媒AcetoneHCID 180—
生成物Amides, C5-9, N-(3-(dimethylamino)propyl)HCID 34925586.8%

反応条件

温度5 °C

反応手順

A 51.1 g (0.50 mol) portion of N,N-dimethyl-1,3-diaminopropane was put into a flask and cooled to 5° C. while stirring in an atmosphere of nitrogen. Under ice-cooling, to this was added dropwise 51.1 g (0.50 mol) of acetic anhydride spending 1 hour. After completion of the dropwise addition, this was further stirred at 25° C. for 3 hours. Thereafter, the reaction mixture was again ice-cooled and 41.6 g (0.5 mol) of 48% sodium hydroxide aqueous solution was added dropwise thereto spending 15 minutes and then, after completion of the dropwise addition, 350 ml of acetone was added to the reaction mixture and allowed to stand at room temperature for 8 hours. Sodium acetate precipitated in the acetone solution was removed by filtration, acetone was evaporated under a reduced pressure and then 71 g of the remaining yellow oil was distilled under a reduced pressure to obtain the title compound as a transparent oil. Yield 62.4 g (0.433 mol; yield 86.8%, boiling point 116-118° C./0.64 kPa).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06586639B2
出典データセットuspto-grants-2003_07
ORD IDord-a5bc1d439c6a4ddba438b5838ffd732b
出典メモuspto-grants-2003_07