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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727387Generated: October 25, 2026

2-Chlorobenzoyl chloride → 5-(2-Chlorobenzamido)-4-(2-chlorobenzoyl)-3-methyl-1-(2,4,6-trichlorophenyl)pyrazole

https://huagongshe.com/reaction/727387

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorobenzoyl chlorideHCID 69110—
Reactant3-Methyl-1-(2,4,6-trichlorophenyl)-1H-pyrazol-5-amineHCID 2060032—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,1,2,2-TetrachloroethaneHCID 6591—
Product5-(2-Chlorobenzamido)-4-(2-chlorobenzoyl)-3-methyl-1-(2,4,6-trichlorophenyl)pyrazoleHCID 1842779251.2%

Reaction Steps

A suspension of 2.34 g (17.50 mmol) of aluminum trichloride in 20 mL of 1,1,2,2-tetrachloroethane was treated with 2.02 mL (2.78 g, 15.9 mmol) of 2-chlorobenzoyl chloride and the resulting solution was stirred for 20 minutes at room temperature. Then 2.00 g (7.23 mmol) of the product of Step A was added and the reaction mixture was refluxed for 16 hours. The cooled reaction mixture was poured over ice and the insolubles were filtered off and washed with ethyl acetate. The organic layer was separated and the aqueous was washed twice with ethyl acetate. The combined organic layers were dried over magnesium sulfate and evaporated. The residues were chromatographed on silica gel, eluting with 4:1 hexane ethyl acetate to give 2.05 g (51%) of the title product, an amorphous foam. Anal. Calcd. for C24N14O2N3Cl5 : C, 52.06; H, 2.55; N, 7.59. Found: C, 52.11; H, 2.57; N, 7.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712303
Source datasetuspto-grants-1998_01
ORD IDord-00aff6261ec046d3a6549c48b117080f
Source noteuspto-grants-1998_01