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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11432Generated: October 26, 2026

Hydrochloric Acid → 2-(1Adamantyl)-n-pentylethylamine hydrochloride

https://huagongshe.com/reaction/11432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium IodideHCID 5238—
ReactantPentylamineHCID 8060—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(1-Adamantyl)ethyl methanesulfonateHCID 15717682—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product2-(1Adamantyl)-n-pentylethylamine hydrochlorideHCID 49831680—

Reaction Steps

Pentylamine (2.69 ml, 23.2 mmol), potassium carbonate (2.14 g, 15.5 mmol) and sodium iodide (2.30 g, 15.3 mmol) were added to a solution of 2-(1-adamantyl)ethyl methanesulfonate (2.07 g, 8.01 mmol) in ethanol (45.8 ml), and the mixture was refluxed for 17 hours. The reaction mixture was concentrated under reduced pressure, and the concentrate was diluted with chloroform (100 ml). This was washed with a 1 N aqueous sodium hydroxide solution (100 ml) and a saturated aqueous sodium chloride solution (100 ml) successively, and the organic layer was dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography. A 4 N solution of hydrogen chloride in ethyl acetate (3.1 ml) was added to a solution of the resulting free form (1.52 g, 6.10 mmol) of the titled compound in ethyl acetate (0.50 ml). The precipitated solid was washed with ethyl acetate and filtered off to give 1.33 g (60%) of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098226B2
Source datasetuspto-grants-2006_08
ORD IDord-0be30f756b24468c9c36d5c24ba0fe57
Source noteuspto-grants-2006_08