Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324598Generated: October 30, 2026

Hydrochloric Acid → Tert-butyl 2,4-dioxo-1,3,8-triazaspiro[4.5]decane-8-carboxylate

https://huagongshe.com/reaction/324598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CyanideHCID 9032—
ReactantAmmonium CarbonateHCID 517111—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantWater ethanolHCID 19096565—
ProductTert-butyl 2,4-dioxo-1,3,8-triazaspiro[4.5]decane-8-carboxylateHCID 3629994—

Reaction Conditions

Temperature60 °C

Reaction Steps

2.12 g (32.6 mmol) of potassium cyanide are added to a solution of 5 g (25.1 mmol) of N-tert-butoxycarbonyl-4-piperidone (34.1) and 24.01 g (250 mmol) of ammonium carbonate in 80 ml of EtOH/water=1/1 and the mixture is left to stir at 60° C. for 5 h. The pH is subsequently adjusted to 6.3 by adding 6N HCl and the mixture is stirred at 60° C. for a further 1.5 h. The precipitate is filtered off with suction and dried under high vacuum. 3.43 g of (34.2) are obtained as a colorless solid. A further 1.0 g of (34.2) is obtained by extracting the filtrate with dichloromethane, drying the organic phase over sodium sulfate, filtering and removing the solvent in vacuo. Total yield of (34.2): 4.43 g (66%) of colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218415B1
Source datasetuspto-grants-2001_04
ORD IDord-b44b7836309b4e4c9670b3aae5b9b551
Source noteuspto-grants-2001_04