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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1356707Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1356707

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
EduktN,N-Dimethyl-1,3-propanediamineHCID 7993—
EduktSodium HydroxideHCID 14798—
LösungsmittelAcetoneHCID 180—
ProduktAmides, C5-9, N-(3-(dimethylamino)propyl)HCID 34925586,8%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06586639B2
Quelldatensatzuspto-grants-2003_07
ORD IDord-a5bc1d439c6a4ddba438b5838ffd732b
Quellennotizuspto-grants-2003_07