HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29081Erstellt: 24. Oktober 2026
Methanamine, N-methoxy-, hydrochloride (1:1) → 4,4,N-Trimethoxy-N-methylbutyramide
https://huagongshe.com/de/reaction/29081
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Edukt | Methyl 4,4-dimethoxybutanoate | HCID 350846 | — |
| Edukt | HCID 178418918 | HCID 178418918 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4,4,N-Trimethoxy-N-methylbutyramide | HCID 59788083 | 100,2% |
Reaktionsschritte
To a solution of methyl 4,4-dimethoxy-butyrate(4.99 g, 30.8 mmol) and N,O-dimethylhydroxylamine HCl(4.65 g, 47.68 mmol) in 60 mL of THF at −20° C., is added isopropylmagnesiumchloride(46 mL, 92.28 mmol, 2.0M in THF) maintaining the temperature below −20° C. After stirring at −10° C. for 30 min, the reaction mixture is quenched with 50 mL of water and extracted with 3×80 mL of EtOAc. The combined organic layers is dried over Na2SO4 and filtered through a short silica gel pluge. The solution is concentrated to give 4,4,N-Trimethoxy-N-methyl-butyramide(5.9 g, 99%) as pale liquid. M/Z=191.0
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07419975B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-2b6194763bc54e6c963c0d78501603e1 |
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| Quellennotiz | uspto-grants-2008_09 |
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