HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061009Generated: November 1, 2026
Phosphorus pentachloride → phenyl 2-methyl-N-phenyl-3-(phenylthio)thioacrylimidate
https://huagongshe.com/reaction/2061009
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | (E)-2-methyl-N-phenyl-3-(phenylthio)-2-propenamide | HCID 59498330 | — |
| Reactant | Sodium benzenethiol | HCID 66586497 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | phenyl 2-methyl-N-phenyl-3-(phenylthio)thioacrylimidate | HCID 67543149 | 36.9% |
Reaction Steps
To a suspension of 0.8 g (3 mmol) of (E)-2-methyl-N-phenyl-3-(phenylthio)-2-propenamide in toluene (4 ml) was added 0.62 g (3 mmol) of phosphorus pentachloride and the mixture was stirred at room temperature for 4 hours. After concentration of the mixture under vacuum, the residue was dissolved in 35 ml of N,N-dimethylformamide [DMF] and then 793 mg (6 mmol) of a benzenethiol sodium salt was added portionwise under ice cooling. The mixture was stirred at room temperature for 2 hours. After dilution with tert-butyl methyl ether, the mixture was washed sequentially with water (three times) and saturated NaCl solution, dried over anhydrous MgSO4, and concentrated under vacuum. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=20/1) to obtain 0.4 g of phenyl 2-methyl-N-phenyl-3-(phenylthio)-2-propenimidothioate (hereinafter referred to as the present compound 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08278473B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-5716523af6894a709898f1277332beef |
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| Source note | uspto-grants-2012_10 |
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