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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 42757Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/42757

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylene GlycolHCID 174—
EduktNitrogenHCID 947—
EduktTrimethyl orthoformateHCID 9005—
EduktSodium CarbonateHCID 10340—
Edukt3'-BromoacetophenoneHCID 16502—
Produkt2-(3-Bromophenyl)-2-methyl-1,3-dioxolaneHCID 10999218—

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536209B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-2395729cc9094f8db19164bab0b1ef65
Quellennotizuspto-grants-2013_09