Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790422Generated: October 26, 2026

Ethylene Glycol → Ethyl 8-benzyl-1,4-dioxa-8-azaspiro[4.5]decane-6-carboxylate

https://huagongshe.com/reaction/1790422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantEthyl 1-benzyl-4-oxopiperidine-3-carboxylateHCID 102624—
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventTolueneHCID 1140—
ProductEthyl 8-benzyl-1,4-dioxa-8-azaspiro[4.5]decane-6-carboxylateHCID 2203823666%

Reaction Steps

p-Toluenesulfonic acid monohydrate (1.5 g) was added to a solution (600 ml) of ethyl 1-benzyl-4-oxo-3-piperidinecarboxylate (CAS Registry No. 1454-53-1, 44.7 g) and ethylene glycol (100 ml) in toluene and the resultant mixture was heated under reflux overnight. After cooling the mixture to room temperature, ice water (500 ml) and a saturated aqueous solution (300 ml) of sodium bicarbonate were added thereto followed by extraction with ethyl acetate (400 ml) for three times. The organic phase was washed successively with water (200 ml) twice and brine (300 ml) and dried over anhydrous magnesium sulfate. The residue was purified by silica gel column chromatography (hexane/ethyl acetate system) to give the title compound (30.4 g) as a yellow oil (yield: 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071201B2
Source datasetuspto-grants-2006_07
ORD IDord-d3ee222fd0f34ea4b9b1ada4fc613bdb
Source noteuspto-grants-2006_07