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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75154Generated: October 26, 2026

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

https://huagongshe.com/reaction/75154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTricyclo(3.3.1.13,7)dec-1-ylmethylamineHCID 86625—
Reactant2,2-Dimethyl-5-(3-methylbutanoyl)-1,3-dioxane-4,6-dioneHCID 59437173—
Solvent1,4-DioxaneHCID 31275—
ProductN-(1-adamantylmethyl)-5-methyl-3-oxohexanamideHCID 5943716254.4%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835426B2
Source datasetuspto-grants-2014_09
ORD IDord-0ecc176c213940abade3d063b7446509
Source noteuspto-grants-2014_09