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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635817Generated: October 30, 2026

4-Chlorobenzoyl chloride → 2-Chloro-1-[4-(4-chlorobenzoyl )-1-methyl-1H-pyrrol-2-yl]-ethanone

https://huagongshe.com/reaction/635817

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
Reactant2-Chloro-1-(1-methyl-1H-pyrrol-2-yl)-ethanoneHCID 2512404—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichloroethaneHCID 11—
Product2-Chloro-1-[4-(4-chlorobenzoyl )-1-methyl-1H-pyrrol-2-yl]-ethanoneHCID 1049412849.2%

Reaction Steps

solution of 30 g (0.19 mole) of 2-chloro-1-(1-methyl-1H-pyrrol-2-yl)-ethanone (10) in 180 mL 1,2-dichloroethane (DCE) under an argon atmosphere was cooled in an ice bath and 60 g AlCl3 (0.45 mole) was added in portions. After stirring for 10 minutes, a solution of 24 mL (0.19 mole) 4-chlorobenzoyl chloride in 110 mL DCE was added dropwise. The ice bath was removed and the reaction was stirred at room temperature overnight. The reaction was poured into 1N HCl/ice and the aqueous layer was extracted three times with methylene chloride. The organics solutions were combined, washed with water, 1N NaOH, water, brine, and dried (MgSO4). Evaporation of the solvent in vacuo gave a solid which was recrystallized from ethyl acetate/methylcyclohexane to give 27.67 g of a solid: mp 130-132° C.; NMR 300 MHz (CDCl3) d 7.8 (m, 2H); 7.6-7.4 (m, 4H); 4.5 (s, 2H); 4.0 (s, 3H). Anal Calcd for C14H11Cl2NO2: C, 56.78; H, 3.74; N, 4.73. Found: C, 56.72; H, 3.76; N, 4.73.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06191142B1
Source datasetuspto-grants-2001_02
ORD IDord-8c9752c373934c26876dc7a6806b4855
Source noteuspto-grants-2001_02