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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064978Generated: October 31, 2026

Ethylene Glycol → 2-(3-Bromophenyl)-2-methyl-1,3-dioxolane

https://huagongshe.com/reaction/2064978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantNitrogenHCID 947—
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium CarbonateHCID 10340—
Reactant3'-BromoacetophenoneHCID 16502—
Product2-(3-Bromophenyl)-2-methyl-1,3-dioxolaneHCID 10999218—

Reaction Conditions

Temperature95 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 1-(3-bromo-phenyl)-ethanone (1360 mg, 6.83 mmol) in ethylene glycol (8.00 mL, 143.46 mmol) was treated with trimethylorthoformate (1.50 mL, 13.68 mmol) followed by LiBF4 (131 mg, 1.37 mmol). The reaction mixture was heated at 95° C. for 15 h. Sat. aq. Na2CO3 was added and the mixture was extracted twice with ether and the combined organic extracts were dried over Na2SO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (20:1 hept-EA) gave the title compound as a pale yellow oil. TLC: rf (10:1 hept-EA)=0.34. LC-MS-conditions 02: tR=1.01 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288419B2
Source datasetuspto-grants-2012_10
ORD IDord-4883d9eaa53f40e5b5b6e20440003cfb
Source noteuspto-grants-2012_10