Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 39683Erstellt: 24. Oktober 2026

Methanol → 1-[(2-Bromoethyl)sulfanyl]-3-fluorobenzene

https://huagongshe.com/de/reaction/39683

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt1,2-DibromoethaneHCID 7839—
Eduktm-FluorobenzenethiolHCID 75710—
EduktSodium methanolate methanolHCID 23694274—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-[(2-Bromoethyl)sulfanyl]-3-fluorobenzeneHCID 22470626—

Reaktionsschritte

To 2 mL of a methanol solution containing 0.83 g of 28% sodium methoxide/methanol, 1.0 mL of 1,2-dibromoethane and 0.50 g of 3-fluorobenzenethiol were added under cooling with ice, the mixture was stirred at the same temperature for 1 hour, at room temperature for 2 hours, and at 50° C. for 1 hour, and then the reaction mixture was refluxed by heating for 5 hours. The reaction mixture was cooled to room temperature, and then ethyl acetate and water were added thereto. The organic layer was separated, washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent; hexane] to obtain 0.62 g of a pale yellow oily substance, 1-(3-fluorophenyl)thio-2-bromoethane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524738B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-4c599ba040dc492a8ebc1ad9adb1f598
Quellennotizuspto-grants-2013_09