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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414545Generated: October 31, 2026

Dimethyl Sulfoxide → HCID 70578562, compound

https://huagongshe.com/reaction/1414545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantXantheneHCID 7107—
Reactant2-Chloroethyl vinyl etherHCID 8074—
ReactantSodium hydrideHCID 24758—
ReactantSodiumHCID 5360545—
SolventWaterHCID 962—
ProductHCID 70578562HCID 70578562—

Reaction Steps

A solution of xanthene (18.2 g.) in dimethyl sulphoxide (150 ml.) is added dropwise over 20 minutes at room temperature to a solution of sodium methylsulphinylmethide [prepared in the usual way from sodium hydride (12 g. of a 60% dispersion in mineral oil) and dimethyl sulphoxide (150 ml.)] with stirring in an atmosphere of nitrogen. The blood-red mixture is stirred at room temperature for a further 30 minutes, cooled to 10° C., and 2-chloroethyl vinyl ether (21.3 g.) is then added dropwise during 30 minutes. Water (750 ml.) is added to the now colourless mixture, and the mixture is extracted three times with ether. The combined ether extracts are dried over MgSO4 and evaporated to dryness. The residue of 9,9-bis(2'-vinyloxyethyl)xanthene (28.0 g.) is dissolved in acetone (150 ml.) and treated with excess Jones reagent (chromic acid in acetone) at 10° C. Methanol is then added, and the solvent is evaporated. To the residue water is added, and the mixture is extracted three times with ethyl acetate. The combined extracts are washed with saturated sodium hydrogen carbonate solution, then with water, dried over MgSO4 and evaporated to dryness. The solid residue is recrystallised from ethanol to give xanthene-9-spiro-4'-tetrahydropyran-2'-one, m.p. 156°-159° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04001419
Source datasetuspto-grants-1977_01
ORD IDord-f6b21e8f7cbb4cb79f25c059996741d2
Source noteuspto-grants-1977_01