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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75147Generated: October 26, 2026

Tricyclo(3.3.1.13,7)dec-1-ylmethylamine → 1-(4-(Benzyloxy)phenyl)-2-((1-adamantylmethyl)amino)ethanol

https://huagongshe.com/reaction/75147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTricyclo(3.3.1.13,7)dec-1-ylmethylamineHCID 86625—
Reactant2-[4-(Benzyloxy)phenyl]oxiraneHCID 13248717—
SolventIsopropanolHCID 3776—
Product1-(4-(Benzyloxy)phenyl)-2-((1-adamantylmethyl)amino)ethanolHCID 5943717623.2%

Reaction Steps

2-(4-(benzyloxy)phenyl)oxirane (2 g, 8.8 mmol) and (1-adamantylmethyl)amine (1.46 g, 8.8 mol) were dissolved in isopropyl alcohol (30 mL) and heated under reflux overnight. The mixture was concentrated to give the crude product, which was purified by column chromatography to afford 1-(4-(benzyloxy)phenyl)-2-((1-adamantylmethyl)amino)ethanol (0.8 g, 23%). 1H NMR: (CDCl3, 400 MHz) δ=1.51 (m, 6H), 1.60-1.72 (m, 6H), 1.97 (m, 3H), 2.32&2.45 (dd, 2H), 2.64 (m, 1H), 2.73 (m, 1H), 2.94 (m, 1H), 3.40 (brs, 3H), 4.79 (m, 1H), 6.93 (m, 2H), 7.26-7.43 (m, 7H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835426B2
Source datasetuspto-grants-2014_09
ORD IDord-88047b6c7522438b9fa11d82686d0f95
Source noteuspto-grants-2014_09