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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871611Generated: October 26, 2026

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

https://huagongshe.com/reaction/1871611

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 C24H14O2N3Cl5 : 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 numberUS06103900
Source datasetuspto-grants-2000_08
ORD IDord-eda38d0d8c7b44b381ecbb1e134e1a2d
Source noteuspto-grants-2000_08