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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701518Generated: October 30, 2026

Benzoyl chloride, 3-chloro- → HCID 12783775, compound

https://huagongshe.com/reaction/1701518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3-chloro-HCID 69252—
ReactantMethyl 1-methylpyrrole-2-carboxylateHCID 142178—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 12783775HCID 1278377594.5%

Reaction Conditions

Temperature5 °C

Reaction Steps

To 100 ml 1,2-dichloroethane are added 5 g 3-chloro-benzoyl chloride followed by 8.4 g aluminium chloride. The mixture is cooled to 5° C. and 4 g methyl 1-methylpyrrole-2-carboxylate dissolved in 15 ml 1,2-dichloroethane are added thereto. The resulting mixture is stirred 0.5 hour at said temperature and then 1 hour at room temperature, after which the solution is hydrolyzed over ice, the organic phase is decanted and the solvent is evaporated off. Recrystallization of the solid residue from methanol give 7.5 g methyl 1-methyl-4-(3-chlorobenzoyl)pyrrole-2-carboxylate, m.p.=126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04194003
Source datasetuspto-grants-1980_03
ORD IDord-3af27fc111fd4880a50a52e356a8685f
Source noteuspto-grants-1980_03