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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437051Generated: October 25, 2026

Potassium Carbonate → 1-(o-Fluorobenzyl)-2[(di-sec-butylamino)acetyl]pyrrole

https://huagongshe.com/reaction/437051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantDI-Sec-butylamineHCID 12277—
Reactant2-Chloro-1-{1-[(2-fluorophenyl)methyl]-1H-pyrrol-2-yl}ethan-1-oneHCID 20391531—
SolventDiethyl EtherHCID 3283—
SolventO-XyleneHCID 7237—
Product1-(o-Fluorobenzyl)-2[(di-sec-butylamino)acetyl]pyrroleHCID 20391558—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 16.0 g of 2-chloroacetyl-1-(o-fluorobenzyl)pyrrole, Example 1a, 8.3 g of di-sec-butylamine and 20.0 g of potassium carbonate in 250 ml xylene is stirred at 120° C. for 72 hours. The mixture is cooled, washed with water, dried and filtered and the xylene is evaporated leaving a brown oil. The oil is dissolved in ether and extracted into a 2N hydrogen chloride solution. The aqueous acidic solution is basified with a sodium carbonate solution and extracted with ether. The ether solution is washed, dried and filtered and the ether removed leaving a brown oil of 1-(o-fluorobenzyl)-2[(di-sec-butylamino)acetyl]pyrrole. Infrared and nuclear magnetic resonance spectra confirm this structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04029672
Source datasetuspto-grants-1977_06
ORD IDord-4510cb9941db4bcf8af22680c94c132b
Source noteuspto-grants-1977_06