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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | N,N-Dimethyl-1,3-propanediamine | HCID 7993 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | Amides, C5-9, N-(3-(dimethylamino)propyl) | HCID 349255 | 86,8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06586639B2 |
|---|
| Quelldatensatz | uspto-grants-2003_07 |
|---|
| ORD ID | ord-a5bc1d439c6a4ddba438b5838ffd732b |
|---|
| Quellennotiz | uspto-grants-2003_07 |
|---|