HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706360Generated: October 30, 2026
3,4-Dichlorophenyl isocyanate → HCID 20335432, compound
https://huagongshe.com/reaction/1706360
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,4-Dichlorophenyl isocyanate | HCID 7607 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(4-Methoxyphenyl)-5-methyl-2,4-dihydro-3H-pyrazol-3-one | HCID 124732 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 20335432 | HCID 20335432 | — |
Reaction Steps
The stirred solution of 4.1 g of 1-(p-methoxyphenyl)-3-methyl-2-pyrazolin-5-one in 75 ml of warm benzene and 2.4 g of triethylamine is combined with the solution of 3.8 g of 3,4-dichlorophenylisocyanate in 50 ml of benzene. After standing at ambient temperature for 4 hours, the benzene is evaporated, the residue taken up in methanol and the solution poured into 100 ml of 0.3 N hydrochloric acid. The mixture is allowed to stand overnight at room temperature, the precipitate is collected, washed with water, dried, triturated with benzene-ethyl acetate and recrystallized from methanol to yield the 1-(p-methoxyphenyl)-3-methyl-4-(3,4-dichlorophenylcarbamoyl)-2-pyrazolin-5-one of Formula II with R=OCH3, R'=3--Cl and R"=Cl, melting at 120°-125°, resolidifying and remelting at 228°-232° (dec.).
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-76218720fce94a4dabcb56925f1b8c9b |
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| Source note | uspto-grants-1980_06 |
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