Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 53914774 | HCID 53914774 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14892625 | HCID 14892625 | 94% |
Reaction Steps
1-Methylsulfinyl-1-methylthio-2-phenylethylene (1.154 g) was dissolved in 15 ml of methylene chloride, and 1 ml of triethylamine was added. Under cooling at -15° C., 0.55 ml of phosphorus oxychloride was added. The mixture was stirred at -15° C. for 1 hour and then at room temperature for 2 hours. Water (30 ml) was added, and the reaction mixture was extracted three times with 30 ml of methylene chloride. The organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was chromatographed on a Florisil column using hexane/benzene as an eluant to afford 1.180 g of 1,1-bis(methylthio)-2-chloro-2-phenylethylene in a yield of 94%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04144248 |
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| Source dataset | uspto-grants-1979_03 |
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| ORD ID | ord-98114c1658854475883afca3e2d1a1b4 |
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| Source note | uspto-grants-1979_03 |
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