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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189404Generated: October 29, 2026

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

https://huagongshe.com/reaction/1189404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantNitrogenHCID 947—
ReactantTrimethyl orthoformateHCID 9005—
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 3′-bromoacetophenone (4.67 mL, 33.89 mmol) in ethylene glycol (36.4 mL) was treated with trimethylorthoformate (7.58 mL, 69.14 mmol) followed by LiBF4 (648 mg, 6.78 mmol). The reaction mixture was heated at 95° C. for 3.5 h. The reaction mixture was cooled to rt and partitioned between ether (100 mL) and sat. aq. Na2CO3 (25 mL). The layers were separated and the aq. layer extracted twice with ether (50 mL). The combined org. extracts were dried over Na2SO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (9:1 hept-EA) gave the title compound as a dark yellow oil. TLC: rf (9:1 hept-EA)=0.44. LC-MS-conditions 02: tR=1.00 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674111B2
Source datasetuspto-grants-2014_03
ORD IDord-74d6f94912b9441980cb8207ddc13e0f
Source noteuspto-grants-2014_03