HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 968153Erstellt: 24. Oktober 2026
Methanol → N-(3-Amino-2,2-dimethylpropyl)-1-amino-1,1-dimethyl-2-butanone oxime
https://huagongshe.com/de/reaction/968153
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | 2,2-Dimethyl-1,3-propanediamine | HCID 81770 | — |
| Edukt | 2-Chloro-2-methyl-3-nitrosobutane | HCID 10866386 | — |
| Produkt | N-(3-Amino-2,2-dimethylpropyl)-1-amino-1,1-dimethyl-2-butanone oxime | HCID 87946981 | — |
Reaktionsschritte
To a solution of 2,2-dimethyl-1,3-propane diamine (69 g, 0.75 mole) in dry methanol (100 mL), 3-chloro-3-methyl-2-nitrosobutane (20.55 g, 0.15 mole, Example 1) was added in portions at 0° C. over a period of 2 hours. The reaction mixture was then stirred at room temperature for 20 hours. The solvent was removed under reduced pressure to give a paste. Water (50 mL) was added, and the solution was cooled in an ice bath. The solution was filtered and the filtrate was adjusted to pH 10-11 by the addition of sodium hydroxide. The solution was cooled again and filtered. The filtrate was concentrated under reduced pressure to a paste and then extracted with ether repeatedly (10×50 mL). The combined ether solution was concentrated to give an oil which was recrystallized twice from petroleum ether to yield the title A compound as a colorless crystalline solid (20.0 g), m.p. 58-60° C. 1H NMR [CDCl3]: δ 0.85 (s, 6H, C-Me2), 1.28 (s, 6H, N—CMe2), 1.9 (s, 3H, N═CMe), 2.2 (s, 2H, NCH2) and 2.6 (s, 2H, N—CH2).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06958141B2 |
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| Quelldatensatz | uspto-grants-2005_10 |
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| ORD ID | ord-000200069bf6430a92a535f513fc7b6f |
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| Quellennotiz | uspto-grants-2005_10 |
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