HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460736Generated: October 29, 2026
Hydrochloric Acid → 1-(2,4,6-Trichlorophenyl)-2-acetyl-3-(2-chloro-5-myristoylaminoanilino)-3-pyrazolin-5-one
https://huagongshe.com/reaction/460736
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | N-[4-chloro-3-[[5-oxo-1-(2,4,6-trichlorophenyl)-4H-pyrazol-3-yl]amino]phenyl]tetradecanamide | HCID 178443172 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2,4,6-Trichlorophenyl)-2-acetyl-3-(2-chloro-5-myristoylaminoanilino)-3-pyrazolin-5-one | HCID 21394050 | — |
Reaction Steps
1.07 g (0.01 mole) of lutidine is added to a solution of 30.7 g (0.05 mole) of 1-(2,4,6-trichlorophenyl)-3-(2-chloro-5-myristoylaminoanilino)-2-pyrazolin-5-one and 8 g (0.06 mole) of anhydrous aluminium chloride in 100 ml of dichloromethane. The solution is cooled to 10° C and 5.90 g (0.075 mole) of acetylchloride are added. 8 g (0.075 mole) of lutidine divided into 4 portions of 2 g each (one portion every 15 min) are added in a total period of time of 1 h, the temperature being kept below 10° C. The reaction mixture is stirred for 2 h more and then poured out into 1 l of 1N aqueous hydrochloric acid. The dichloromethane layer is washed until free from acid, dried, and concentrated by evaporation. The product is agitated with methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04061498 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-1e047ed0942046248435f195249898c6 |
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| Source note | uspto-grants-1977_12 |
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