HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Tricyclo(3.3.1.13,7)dec-1-ylmethylamine → N-(1-adamantylmethyl)-5-methyl-3-oxohexanamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Tricyclo(3.3.1.13,7)dec-1-ylmethylamine | HCID 86625 | — |
| Edukt | 2,2-Dimethyl-5-(3-methylbutanoyl)-1,3-dioxane-4,6-dione | HCID 59437173 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | N-(1-adamantylmethyl)-5-methyl-3-oxohexanamide | HCID 59437162 | 54,4% |
Reaktionsschritte
A solution of 5-(3-methylbutanoyl)-2,2-dimethyl-1,3-dioxane-4,6-dione (2.76 g, 12 mmol) and (1-adamantylmethyl)amine (2 g, 12 mmol) in anhydrous 1,4-dioxane (10 mL) was heated under reflux for 2 h. Solvent was removed in vacuo. The residue was diluted with EtOAc (50 mL), washed with water, aq K2CO3 and brine, dried over Na2SO4 and concentrated to dryness. The residue was purified by chromatography on a silica gel column eluted with 20:1 PE/EtOAc to give the N-(1-adamantylmethyl)-5-methyl-3-oxohexanamide (1.90 g, 54.4%). 1H NMR: (400 MHz, CDCl3): δ=0.92 (s, 3H), 0.96 (s, 3H), 1.54 (s, 7H), 1.62-1.73 (m, 9H), 1.98 (s, 4H), 2.12(m, 1H), 2.45(d, 2H), 2.95(d, 2H), 3.65(s, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08835426B2 |
| Quelldatensatz | uspto-grants-2014_09 |
| ORD ID | ord-0ecc176c213940abade3d063b7446509 |
| Quellennotiz | uspto-grants-2014_09 |