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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863446Generated: October 27, 2026

Hydrochloric Acid → 2-Chloroacetyl-1-(o-fluorophenethyl)pyrrole

https://huagongshe.com/reaction/1863446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloroacetonitrileHCID 7856—
Reactant1-[(2-Fluorophenyl)methyl]-1H-pyrroleHCID 14391472—
Reactant2-Chloro-1-{1-[(2-fluorophenyl)methyl]-1H-pyrrol-2-yl}ethan-1-oneHCID 20391531—
SolventDiethyl EtherHCID 3283—
Product2-Chloroacetyl-1-(o-fluorophenethyl)pyrroleHCID 20391533—
Producto-FluorophenethylpyrroleHCID 54477722—

Reaction Steps

A solution of 40 g of 1-(o-fluorobenzyl)pyrrole and 17.2 g of chloroacetonitrile in 200 ml of anhydrous ether at a temperature between 0° and -5° C. is saturated with hydrogen chloride gas and then the solution is stirred until a heavy white cake forms. This cake is broken up and permitted to sit for one hour at ambient temperature. The white solid is filtered, washed with ether and dried and then hydrolyzed in water and extracted with ether. Concentration of the ether extracts leaves white crystals, mp 76°-78° C., of 2-chloroacetyl-1-(o-fluorobenzyl)pyrrole. The analagous treatment of o-fluorophenethylpyrrole produces 2-chloroacetyl-1-(o-fluorophenethyl)pyrrole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04169095
Source datasetuspto-grants-1979_09
ORD IDord-1959c4a870974624b8debbfbdd6f987e
Source noteuspto-grants-1979_09