Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836901Generated: November 1, 2026

Ethylene Glycol → HCID 23498864, compound

https://huagongshe.com/reaction/1836901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 23498870HCID 23498870—
SolventBenzeneHCID 241—
SolventDichloromethaneHCID 6344—
ProductHCID 23498864HCID 23498864—

Reaction Steps

7-Acetoxy-3-bromo-2-formyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene (0.3 g, 0.849 mmol) from the preceding reaction was dissolved in 2 mL of benzene. Ethylene glycol (0.104 mL, 1.87 mmol) and p-toluenesulfonic acid monohydrate (0.024 g, 0.127 mmol) were added. A Dean-Stark apparatus was attached to the reaction flask and the reaction was brought to reflux for several hours. When the reaction was judged complete by TLC (SiO2, 20% ethyl acetate/hexanes), dichloromethane (25 mL) and sodium bicarbonate solution (50 mL) were added and the layers were separated. The aqueous layer was extracted one more time with dichloromethane. The combined organic layers were washed with brine, dried over sodium sulfate and concentrated to give 7-Acetoxy-3-bromo-2-(1,3-dioxolane-2-yl)-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene as an oily residue that was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777418B2
Source datasetuspto-grants-2004_08
ORD IDord-5bcd21c1d60446ca9b90a438dd9b3fd3
Source noteuspto-grants-2004_08