Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811653Generated: November 1, 2026

Water → benzyl(R)-3-[(R)-1-(naphthalen-1-yl)ethylamino]piperidine-1-carboxylate

https://huagongshe.com/reaction/1811653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantbenzyl(R)-3-[chlorocarbonyl-(R)-1-(naphthalen-1-yl)ethylamino]piperidine-1-carboxylateHCID 58973551—
SolventTetrahydrofuranHCID 8028—
Productbenzyl(R)-3-[(R)-1-(naphthalen-1-yl)ethylamino]piperidine-1-carboxylateHCID 5897348651.7%

Reaction Steps

To a solution containing 54.6 g of benzyl(R)-3-[chlorocarbonyl-(R)-1-(naphthalen-1-yl)ethylamino]piperidine-1-carboxylate dissolved in 700 ml of tetrahydrofuran was added 350 ml of water, and the mixture was stirred under reflux for 15 hours. After tetrahydrofuran was evaporated, a saturated aqueous sodium bicarbonate solution and chloroform were added thereto, the mixture was stirred and the liquids were separated. The organic layer was dried and concentrated, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1→0:1) to obtain 24.3 g of benzyl(R)-3-[(R)-1-(naphthalen-1-yl)ethylamino]piperidine-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362274B2
Source datasetuspto-grants-2013_01
ORD IDord-0b5dc2227fa649b4907f32531be23ea6
Source noteuspto-grants-2013_01