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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10662Generated: October 30, 2026

Ethylene Glycol → 2-(5-Bromo-2,4-dimethoxyphenyl)-1,3-dioxolane

https://huagongshe.com/reaction/10662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactant5-Bromo-2,4-dimethoxybenzaldehydeHCID 668346—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventBenzeneHCID 241—
Product2-(5-Bromo-2,4-dimethoxyphenyl)-1,3-dioxolaneHCID 1611605492%

Reaction Steps

Ex-46A: 5-Bromo-2,4-dimethoxybenzaldehyde (4.92 g, 20.1 mmol) was dissolved in benzene (41 mL). Ethylene glycol (3 mL, 54 mmol) and p-toluenesulfonic acid (25 mg, 0.13 mmol) were added and the solution was refluxed with a Dean-Stark trap attached. After 6 h, the reaction was cooled and washed with water (1×20 mL), saturated, aqueous NaHCO3 (1×20 mL), and water (1×20 mL). The organic phase was dried over sodium sulfate, filtered, concentrated, and dried to provide 5.32 g of 2-(5-bromo-2,4-dimethoxy-phenyl)-[1,3]dioxolane as a faint yellow oil which solidified upon standing (92% yield). 1H-NMR (CDCl3) δ 7.67 (s, 1H), 6.47 (s, 1H), 6.06 (s, 1H), 4.11–4.13 (m, 2H), 3.98–4.03 (m, 2H), 3.91 (s, 3H), 3.87 (s, 3H). HRMS (ES+) Calcd. for C11H13BrO4: 289.0075. Found: 289.0077.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094801B2
Source datasetuspto-grants-2006_08
ORD IDord-6e624bf1f72147079f9c2ca4a68268e2
Source noteuspto-grants-2006_08