Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447791Generated: October 26, 2026

Dichloromethane → 1-(Oxan-4-yl)piperidin-4-amine dihydrochloride

https://huagongshe.com/reaction/447791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
ReactantTetrahydro-4H-pyran-4-oneHCID 121599—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventWaterHCID 962—
SolventSodium chloride; waterHCID 57417360—
Product1-(Oxan-4-yl)piperidin-4-amine dihydrochlorideHCID 45156751—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1,1-dimethylethyl 4-piperidinylcarbamate (50 g) was added tetrahydro-4H-pyran-4-one (35.75 g) in dry DCM (1000 ml), then was added sodium triacetoxyborohydride (141 g) portion wise over 10 minutes at about 25° C. The mixture was stirred under nitrogen for about 30 hours, then cooled to 0° C. Water (107 ml) was added portion wise in 20 minutes, followed by saturated aqueous potassium carbonate (178 ml) and saturated brine (178 g in 178 ml). The mixture was stirred for 10 minutes at about 25° C., then the layers were separated and the organic layer washed with saturated brine (3×214 ml). After drying over anhydrous sodium sulphate, the organic layer was concentrated and the residue was treated with 100 ml isopropanol and reconcentrated. The residue was slowly heated to reflux with 11% HCl in isopropanol (200 ml) for 2 hours then cooled to about 25° C. The solid was filtered, and slurry washed with diethyl ether (100 ml), then dried under high vacuum to give the title product (43 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481566B2
Source datasetuspto-grants-2013_07
ORD IDord-5535cb3c210d43fa9ee7ebd3c3e33089
Source noteuspto-grants-2013_07