Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 20458836 | HCID 20458836 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20458824 | HCID 20458824 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04450157 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-1be09dcb0fe44eb7a6fca165733e792c |
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| Source note | uspto-grants-1984_05 |
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