HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753134Generated: November 1, 2026
p-Chlorophenacyl bromide → methyl 4-bromo-1-[2-(4-chlorophenyl)-2-oxoethyl]-1H-pyrrole-2-carboxylate
https://huagongshe.com/reaction/1753134
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Chlorophenacyl bromide | HCID 68303 | — |
| Reactant | Methyl 4-bromo-1H-pyrrole-2-carboxylate | HCID 2763594 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl 4-bromo-1-[2-(4-chlorophenyl)-2-oxoethyl]-1H-pyrrole-2-carboxylate | HCID 67366602 | 55.6% |
Reaction Steps
Methyl 4-bromo-1H-pyrrole-2-carboxylate (250 mg, 1.23 mmol) and 2-bromo-1-(4-chloro-phenyl)-ethanone (315 mg, 1.35 mmol) were dissolved in DMF (50 mL). The reaction mixture was cooled to 0° C. before potassium tert-butoxide (125 mg, 1.11 mmol) was added to the reaction mixture in small portions. The resulting suspension was allowed to warm to room temperature then stirred for 10 min. The reaction mixture was diluted with water (100 mL) and extracted with CH2Cl2 (3×100 mL). The organic layers were combined, dried and concentrated in vacuo to give a residue that was purified using flash chromatography (Biotage SP4, 40 g cartridge, 0-15% EtOAc gradient in n-hexanes) to give the target compound methyl 4-bromo-1-[2-(4-chlorophenyl)-2-oxoethyl]-1H-pyrrole-2-carboxylate (244 mg) contaminated with an impurity. The mixture was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09163029B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-20175e5ff6294096821fd5a22db9ba18 |
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| Source note | uspto-grants-2015_10 |
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