HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706362Generated: October 26, 2026
Benzene → 1-Phenyl-3-methyl-4-(p-methylthiophenylcarbamoyl)-2-pyrazolin-5-one
https://huagongshe.com/reaction/1706362
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene | HCID 241 | — |
| Reactant | Mci-186 | HCID 4021 | — |
| Reactant | 4-(Methylthio)phenyl isocyanate | HCID 2733316 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-Phenyl-3-methyl-4-(p-methylthiophenylcarbamoyl)-2-pyrazolin-5-one | HCID 20335427 | — |
Reaction Steps
The mixture of 2.6 g of 1-phenyl-3-methyl-2-pyrazolin-5-one, 75 ml of benzene, 1.8 g of triethylamine and 2.5 g of p-methylthiophenylisocyanate is stirred at ambient temperature and allowed to stand overnight. It is evaporated; the residue taken up in methanol, the solution is filtered and combined with the mixture of 10 ml of 5 N hydrochloric acid and 250 ml of water. The precipitate formed is collected, washed with water, dried, triturated with diethyl ether and dissolved in 2 N aqueous sodium hydroxide. The solution is filtered, acidified with 5 N hydrochloric acid, the precipitate washed with water, dried, triturated with methanol and recrystallized from ethyl acetate, to yield the 1-phenyl-3-methyl-4-(p-methylthiophenylcarbamoyl)-2-pyrazolin-5-one melting at 196°-199°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04207317 |
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| Source dataset | uspto-grants-1980_06 |
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| ORD ID | ord-a12e771c55984f629a3c92ddb227b09e |
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| Source note | uspto-grants-1980_06 |
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