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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544378Generated: October 31, 2026

Methyl iodide → HCID 20458824, compound

https://huagongshe.com/reaction/544378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodiumHCID 5360545—
ReactantHCID 20458836HCID 20458836—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
ProductHCID 20458824HCID 20458824—

Reaction Conditions

Temperature0 °C

Reaction Steps

6.0 g (0.041 mol) of 2,2-dimethyl-thiazolidine-4-thione are added cautiously to a suspension of 1.0 g (0.041 mol) of oil-free sodium hydridein 20 ml of absolute dimethylformamide. After completion of the evolution of hydrogen, the mixture is heated briefly to 50° C., then cooled to 0° C. and 2.6 ml (0.042 mol) of methyl iodide are added dropwisethereto. After removing the ice-bath the mixture is stirred for an additional 3 hours, treated with water and extracted twice with methylene chloride. The organic extracts are subsequently combined, washed three times with 100 ml of water each time, dried over anhydrous sodium sulfate and evaporated at 40° C. under reduced pressure to yield crude 2,2-dimethyl-4-methylthio-3-thiazoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04450157
Source datasetuspto-grants-1984_05
ORD IDord-1be09dcb0fe44eb7a6fca165733e792c
Source noteuspto-grants-1984_05