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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684267Generated: October 27, 2026

Ethylene Glycol → Methyl 1,4-dioxaspiro[4.5]decane-7-carboxylate

https://huagongshe.com/reaction/1684267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantMethyl 3-oxocyclohexane-1-carboxylateHCID 566099—
SolventTolueneHCID 1140—
SolventToluene waterHCID 22272177—
ProductMethyl 1,4-dioxaspiro[4.5]decane-7-carboxylateHCID 372311—

Reaction Conditions

Temperature95 °C

Reaction Steps

A solution composed of 30 g (192 mmol) of crude methyl 3-oxocyclohexanecarboxylate and 430 cm3 of toluene is introduced into a one-liter three-necked flask equipped with a Dean and Stark apparatus, and 14.3 g (230 mmol) of ethylene glycol are then added with 814 mg (4.3 mmol) of para-toluenesulfonic acid monohydrate. The mixture is heated to reflux, the toluene-water azeotrope forms instantaneously and, after 40 min, no further refluxing of azeotrope (95° C.) takes place. The mixture is maintained for 6 h under reflux of the toluene (110° C.). After cooling, sodium hydrogen carbonate solution is added and the solution is then washed with saturated sodium chloride solution and dried over sodium sulfate. After concentration, 39 g of a yellow oil are obtained, which product is either distilled or chromatographed on a column of 215 g of silica (eluant: cyclo-hexane/ether, 98:2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639902
Source datasetuspto-grants-1997_06
ORD IDord-33d9c668b6f747bc98779db9235d35f4
Source noteuspto-grants-1997_06