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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565608Generated: October 24, 2026

Triethylamine → 1-Oxa-3,8-diazaspiro(4.5)decan-2-one, 8-benzyl-

https://huagongshe.com/en/reaction/565608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Aminomethyl)-1-benzylpiperidin-4-olHCID 10421026—
ReactantPhosgen tolueneHCID 19083224—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product1-Oxa-3,8-diazaspiro(4.5)decan-2-one, 8-benzyl-HCID 199815—

Reaction Steps

To a solution of crude 1-benzyl-4-hydroxy-4-aminomethyl piperidine, as described above in Step A, (˜3.1 gm, 12 mmol) in acetonitrile (50 mL) containing triethyl amine (5.7 mL, 42 mmol) cooled in an ice bath was added in 1 mL portions 20% phosgene/toluene (9 mL) over a three hour period. The reaction mixture was stirred at ambient temp. for 15 hours and diluted with ethyl acetate. This solution was washed with water (2×) and the organic layer dried (anhyd. sodium sulfate), filtered, and the solvent removed under vacuum. The residue was triturated with diethyl ether and the title compound collected by filtration as a white solid, mp: 159-161° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172076B2
Source datasetuspto-grants-2001_01
ORD IDord-52baa319d75b4b72b9b4abc10cab7d1f
Source noteuspto-grants-2001_01