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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418375Generated: October 31, 2026

1,4-Dioxa-8-azaspiro(4.5)decane → (3-Methyl-1,2,4-oxadiazol-5-yl)-4-piperidone ethylene ketal

https://huagongshe.com/reaction/1418375

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
Reactant3-Methyl-5-(trichloromethyl)-1,2,4-oxadiazoleHCID 70953—
SolventEthanolHCID 702—
Product(3-Methyl-1,2,4-oxadiazol-5-yl)-4-piperidone ethylene ketalHCID 5715376819.5%

Reaction Steps

3-Methyl-5-trichloromethyl-1,2,4-oxadiazole (Moussebois and Eloy, Helv. Chim. Acta 1964, 47, 838) (1 g, 5 mmol) and 4-piperidone ethylene ketal (1.5 g, 10 mmol) in ethanol (20 ml) were heated reflux overnight. The solvent was evaporated and the residue taken up in dichloromethane and filtered. The filtrate was washed with dilute HCl, dried over sodium sulphate and evaporated to leave a pale yellow oil (0.22 g). The acid washing was neutralised with solid sodium bicarbonate and extracted with dichloromethane. Evaporation gave further oil (0.17 g, total 0.39 g), MS (+EI) 225 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883102
Source datasetuspto-grants-1999_03
ORD IDord-13487dec1f804d92a366f3492c25bde9
Source noteuspto-grants-1999_03