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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 546770Erstellt: 25. Oktober 2026

Dimethyl Sulfoxide → Ethyl (2-fluoro-3-methylphenyl)acetate

https://huagongshe.com/reaction/546770

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktSodium IodideHCID 5238—
EduktEthyl AcetateHCID 8857—
EduktSodium CyanideHCID 8929—
EduktBenzene, 1-(bromomethyl)-2-fluoro-3-methyl-HCID 519062—
LösungsmittelWaterHCID 962—
ProduktEthyl (2-fluoro-3-methylphenyl)acetateHCID 55268648—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A mixture of 2-fluoro-3-methylbenzyl bromide (2.0 g), sodium cyanide (2.41 g), sodium iodide (148 mg) and DMSO (10 ml) was stirred at 60° C. for two hours. Water and ethyl acetate were added to the reaction solution, and the organic layer was separated. The organic layer was washed with brine. The resulting organic layer was dried over anhydrous magnesium sulfate. The organic layer was concentrated under reduced pressure. 5 N hydrochloric acid (15 ml) was added to the residue, and the reaction solution was heated at 110° C. for 22 hours. The reaction solution was brought to room temperature. Chloroform was added and the organic layer was separated. The organic layer was concentrated under reduced pressure. Saturated hydrogen chloride-ethanol (15 ml) was added to the residue, and the reaction solution was stirred at 85° C. for four hours. The reaction solution was concentrated under reduced pressure, and then diluted with ethyl acetate and washed with saturated sodium bicarbonate water and then with brine. The resulting organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain the title compound (1.1 g). The property values of the compound are as follows.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07935815B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-761e8e3a9c9744d3a9e703a7e319a9f4
Quellennotizuspto-grants-2011_05