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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606138Generated: October 26, 2026

Hydrochloric Acid → 5-(2',4'-Dichlorobenzoyl)-1-methylpyrrole-2-acetonitrile

https://huagongshe.com/reaction/1606138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,4-Dichlorobenzoyl chlorideHCID 66645—
Reactant1H-Pyrrole-2-acetonitrile, 1-methyl-HCID 90501—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichloroethaneHCID 11—
Product5-(2',4'-Dichlorobenzoyl)-1-methylpyrrole-2-acetonitrileHCID 18424378—

Reaction Steps

To a suspension of 16.6 g. (0.125 mole) of aluminum chloride in 60 ml. 1,2-dichloroethane is added 26.2 g. (0.125 mole) of 2,4-dichlorobenzoyl chloride. The resulting solution is added slowly to a solution of 15 g. (0.125 mole) of 1-methylpyrrole- 2-acetonitrile in 60 ml. 1,2-dichloroethane while cooling externally with an ice bath. After the addition is complete, the mixture is stirred for 40 minutes at room temperature followed by heating at reflux for 3 minutes. It is then poured into ice acidified with dilute hydrochloric acid. The organic phase is separated and washed successively with N,N-dimethyl-1,3-propanediamine, 3N hydrochloric acid, and saturated sodium chloride solution. It is then dried over magnesium sulfate and the solvent evaporated. The resulting red oily residue is chromatographed on a column packed with neutral alumina and eluted with benzene and ether. The first compound-bearing fractions upon evaporation yield a white solid, 5-(2',4'-dichlorobenzoyl)-1-methylpyrrole- 2-acetonitrile, which is purified by recrystallization from methanol, m.p. 129°-130°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952012
Source datasetuspto-grants-1976_04
ORD IDord-5db331030dec4d2b96f1d125c6d89462
Source noteuspto-grants-1976_04