HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1386524Erstellt: 26. Oktober 2026
Sodium Chloride → N-(2,2-Dimethoxyethyl)-2-propenamide
https://huagongshe.com/reaction/1386524
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Chloride | HCID 5234 | — |
| Edukt | Acryloyl chloride | HCID 13140 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Katalysator | 2,2,6,6-tetramethyl-4-hydroxypiperidine-N-oxide | HCID 11607999 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | N-(2,2-Dimethoxyethyl)-2-propenamide | HCID 9898899 | 81,7% |
Reaktionsschritte
40 g (1.0 mol) of sodium hydroxide are dissolved in 100 g of water and 200 g of ice in a 1 liter reactor fitted with stirring and cooling means. The sodium hydroxide solution is cooled to 10° C., and 105.1 g (1.0 mol) of aminoacetaldehyde dimethyl acetal and 10 mg of the inhibitor 4hydroxy-2,2,6,6-tetramethylpiperidine 1-oxide are added. 995 g (1.1 mol) of acryloyl chloride are slowly added to this solution at 10° C. over the course of 2 hours. The pH drops slowly and is finally set to pH=7. Amine is no longer present according to GC. The reaction mixture is saturated with sodium chloride and extracted three times with 200 ml of tert-butyl methyl ether. The organic phase is dried, filtered and evaporated on a rotary evaporator. The resultant oil is extracted three times with petroleum ether and subsequently re-dried on a rotary evaporator, giving 130 g of acrylamidoacetaldehyde dimethyl acetal (81% of theory) as an oil. The product is 99% pure according to GC.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06265509B1 |
|---|
| Quelldatensatz | uspto-grants-2001_07 |
|---|
| ORD ID | ord-8c56890eb1fd4b2b8e0f4d0de7ccb933 |
|---|
| Quellennotiz | uspto-grants-2001_07 |
|---|