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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1356707생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1356707

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물N,N-Dimethyl-1,3-propanediamineHCID 7993—
반응물Sodium HydroxideHCID 14798—
용매AcetoneHCID 180—
생성물Amides, C5-9, N-(3-(dimethylamino)propyl)HCID 34925586.8%

반응 조건

온도5 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06586639B2
출처 데이터셋uspto-grants-2003_07
ORD IDord-a5bc1d439c6a4ddba438b5838ffd732b
출처 메모uspto-grants-2003_07