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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903Generated: October 26, 2026

Ethylene Glycol → 6-Bromo-1,4-dioxaspiro[4.6]undecane

https://huagongshe.com/reaction/903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantCycloheptanoneHCID 10400—
ReactantBromineHCID 24408—
ReactantSodium BicarbonateHCID 516892—
SolventTetrahydrofuranHCID 8028—
Product6-Bromo-1,4-dioxaspiro[4.6]undecaneHCID 288226—

Reaction Steps

Bromine (44.8 g, 0.28 mol) was added dropwise to a stirred solution of cycloheptanone (28.5 g, 0.25 mol) in a 1:1 solution (300 mL) of ethylene glycol and tetrahydrofuran at room temperature. The mixture was stirred for 5 hours, then poured into aqueous sodium bicarbonate and extracted 3× with diethyl ether. The combined organic layers were washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo to give 2-bromocycloheptanone ethylene ketal (60 g). A mixture of this crude bromo ketal and a methanolic solution of sodium methoxide (250 mL, 25 wt. % solution) was heated at reflux overnight. The mixture was cooled to ambient temperature, poured into water, and extracted with hexanes. The organic layer was washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo to afford 2-cycloheptenone ethylene ketal (39 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723462
Source datasetuspto-grants-1998_03
ORD IDord-c3c99a608b9c4984be003f74893691b4
Source noteuspto-grants-1998_03