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HRID 75154Erstellt: 23. Oktober 2026

Tricyclo(3.3.1.13,7)dec-1-ylmethylamine → N-(1-adamantylmethyl)-5-methyl-3-oxohexanamide

https://huagongshe.com/de/reaction/75154

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTricyclo(3.3.1.13,7)dec-1-ylmethylamineHCID 86625—
Edukt2,2-Dimethyl-5-(3-methylbutanoyl)-1,3-dioxane-4,6-dioneHCID 59437173—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktN-(1-adamantylmethyl)-5-methyl-3-oxohexanamideHCID 5943716254,4%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835426B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-0ecc176c213940abade3d063b7446509
Quellennotizuspto-grants-2014_09