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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585616Generated: November 1, 2026

4-Chlorobenzoyl chloride → HCID 86584041, compound

https://huagongshe.com/reaction/1585616

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 18424250HCID 18424250—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 86584041HCID 86584041—

Reaction Steps

A solution of 13.8 g. (0.0788 mole) of p-chlorobenzoyl chloride and 10.5 g. (0.0788 mole) of aluminum chloride in 120 ml. of 1,2-dichloroethane is added to a refluxing solution of 21.8 g. (0.0788 mole) of ethyl 3-ethoxycarbonyl-4-ethyl-1-methylpyrrole-2-acetate. The mixture is heated under reflux for 10 hours and stirred at room temperature for an additional 10 hours. It is then poured into ice-hydrochloric acid. The organic layer is separated, and the aqueous layer washed with 1,2-dichloroethane. The combined organics are washed successively with water, N,N-dimethylaminopropylamine, dilute HCl and brine. The solution is then dried over anhydrous magnesium sulfate and the solvent evaporated in vacuo. The residual red oily residue crystallizes on standing. It is recrystallized twice from methanol to give ethyl (5-chlorobenzoyl)-3-ethoxycarbonyl-4-ethyl-1-methyl-pyrrole-2-acetate as a white solid, m.p. 72-74° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05939417
Source datasetuspto-grants-1999_08
ORD IDord-e65f6a9195f54076a1eca2cfcd0c56db
Source noteuspto-grants-1999_08