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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279278Generated: October 26, 2026

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

https://huagongshe.com/reaction/1279278

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448265B1
Source datasetuspto-grants-2002_09
ORD IDord-71fd6157abe547ccb36be438f6e5bee6
Source noteuspto-grants-2002_09