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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435685Generated: October 28, 2026

Potassium Iodide → HCID 21481149, compound

https://huagongshe.com/reaction/435685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(2-Chloroethyl)-1,3-oxazolidin-2-oneHCID 75633—
ReactantHCID 21456041HCID 21456041—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
ProductHCID 21481149HCID 21481149—

Reaction Steps

5.9 g of 1-(10,11-dihydro-2-iodo-dibenzo[b,f]thiepin-10-yl)-piperazine are treated, together with 3.3 g of powdered potassium carbonate, 0.07 g of potassium iodide and 40 ml of toluene, with 4.35 g of N-(β-chloroethyl)-oxazolidinone and the mixture is heated under reflux for 27 hours. The mixture is then poured on to water and diluted with chloroform. The organic phase is extracted with 2-N hydrochloric acid. The aqueous phase is made alkaline with sodium hydroxide and extracted with chloroform. The organic phase is dried over magnesium sulphate and concentrated under reduced pressure. The residue is chromatographed over aluminium oxide. There is obtained 3-[ 2-[4-(10,11-dihydro-2-iodo-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl ]-2-oxazolidinone which is converted into the maleate by treatment with maleic acid. The maleate melts at 176°-177° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04006144
Source datasetuspto-grants-1977_02
ORD IDord-45841207dab045c59e18bf7340752796
Source noteuspto-grants-1977_02