HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 924625Erstellt: 26. Oktober 2026
4-Methylmorpholine → 2,2-Dimethyl-N-(2-morpholin-4-yl-ethyl)-Malonamic Acid Ethyl Ester
https://huagongshe.com/reaction/924625
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-Methylmorpholine | HCID 7972 | — |
| Edukt | 3-Ethoxy-2,2-dimethyl-3-oxopropanoic acid | HCID 231754 | — |
| Edukt | 2-Morpholinoethylamine | HCID 408285 | — |
| Edukt | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2,2-Dimethyl-N-(2-morpholin-4-yl-ethyl)-Malonamic Acid Ethyl Ester | HCID 68802054 | — |
Reaktionsschritte
19 g 2,2-Dimethyl-malonic acid monoethyl ester were weighed into a round-bottomed flask and under N2 atmosphere and room temperature, 200 ml tetrahydrofurane, 15.6 ml 4-(2-Aminoethyl)-morpholine and 32.6 ml N-Methylmorpholine were added. The reaction was stirred and cooled down to 5° C. Then, 43.8 g TBTU were added and the mixture was allowed to stir for another 1.5 hours. Finally the solvent was removed and the residue dissolved in 400 ml dichloromethane. This organic phase was washed two times with 500 ml NaHCO3 solution. The dichloromethane phase was dried then the solvent was evaporated. Purity of the product was judged by gas chromatography.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09283186B2 |
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| Quelldatensatz | uspto-grants-2016_03 |
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| ORD ID | ord-457a9135c9e34ee6b321e781a6b88108 |
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| Quellennotiz | uspto-grants-2016_03 |
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