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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728249Generated: October 30, 2026

1,2-Ethanedithiol → Ammonia

https://huagongshe.com/reaction/1728249

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-EthanedithiolHCID 10902—
ReactantSodium HydroxideHCID 14798—
Reactant2,8-Dimethyl-1-oxa-8-azaspiro[4.5]decan-3-oneHCID 10176401—
SolventDichloromethaneHCID 6344—
ProductAmmoniaHCID 222—
ProductHCID 10400364HCID 10400364—

Reaction Steps

A solution of 0.5 g 2,8-dimethyl-1-oxa-8-azaspiro[4,5]-decan-3-one in 10 ml dichloromethane was cooled in ice, 0.45 ml 1,2-ethanedithiol was added, and 2 ml boron trifluoride/ether complex was then added dropwise while maintaining the temperature below 10° C. After stirring at that temperature for one hour, the reaction mixture was poured into 30 ml of 20% aqueous caustic soda solution. The insoluble matters were filtered off, the filtrate was extracted with ethyl acetate, and the organic layer was washed with saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. The dried solution was concentrated under reduced pressure, and the residue was subjected to silica gel column chromatography using, as eluent, a mixed solvent of chloroform/methanol/conc. ammonia (20:1:0.1 by volume), giving 0.46 g of 10,14-dimethyl-13-oxa-1,4-dithia-10-azadispiro[4,1,5,2]tetradecane. It was dissolved in methanol and converted to maleate by addition of an equimolar amount of maleic acid dissolved in the same solvent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE034653
Source datasetuspto-grants-1994_07
ORD IDord-e7a3b59919994cfc9e866458fc8c137f
Source noteuspto-grants-1994_07