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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | DI-Sec-butylamine | HCID 12277 | — |
| Reactant | 2-Chloro-1-{1-[(2-fluorophenyl)methyl]-1H-pyrrol-2-yl}ethan-1-one | HCID 20391531 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 1-(o-Fluorobenzyl)-2[(di-sec-butylamino)acetyl]pyrrole | HCID 20391558 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04029672 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-4510cb9941db4bcf8af22680c94c132b |
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| Source note | uspto-grants-1977_06 |
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