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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437049Generated: October 27, 2026

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

https://huagongshe.com/reaction/437049

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 numberUS04029672
Source datasetuspto-grants-1977_06
ORD IDord-6f7828bd0946419cbd707c831c847ae1
Source noteuspto-grants-1977_06