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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 435689Erstellt: 24. Oktober 2026

Potassium Iodide → 3-[2-[4-(2-Bromo-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl]-2-oxazolidinone

https://huagongshe.com/de/reaction/435689

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktPotassium CarbonateHCID 11430—
Edukt3-(2-Chloroethyl)-1,3-oxazolidin-2-oneHCID 75633—
EduktHCID 21481142HCID 21481142—
LösungsmittelBenzeneHCID 241—
LösungsmittelTolueneHCID 1140—
Produkt3-[2-[4-(2-Bromo-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl]-2-oxazolidinoneHCID 21481155—

Reaktionsschritte

12.5 g of 1-(2-bromo-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-piperazine are treated, together with 13 g of powdered potassium carbonate, 0.2 g of potassium iodide and 1 litre of toluene, with 13.2 g of N-(β-chloroethyl)-oxazolidinone and the mixture is heated under reflux for 25 hours. Then the mixture is poured on to ice-water and diluted with benzene. The benzene solution is washed neutral with water and extracted with 2-N hydrochloric acid. The aqueous phase is made alkaline with sodium hydroxide and extracted with benzene. The organic phase is washed with water, dried over magnesium sulphate and concentrated under reduced pressure. There is obtained crude 3-[ 2-[4-(2-bromo-10,11-dihydro-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl ]-2-oxazolidinone which is converted into the maleate of melting point 170°-172° C by treatment with maleic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04006144
Quelldatensatzuspto-grants-1977_02
ORD IDord-45b9e1119c374046b5630580b9367c5c
Quellennotizuspto-grants-1977_02