HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77354Generated: October 26, 2026
Bromomethyl 4-methoxyphenyl ketone → HCID 67365424, compound
https://huagongshe.com/reaction/77354
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromomethyl 4-methoxyphenyl ketone | HCID 4965 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | ethyl 5-bromo-1H-pyrrole-2-carboxylate | HCID 59559613 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67365424 | HCID 67365424 | 69% |
Reaction Steps
A mixture of ethyl 5-bromo-1H-pyrrole-2-carboxylate (0.13 g, 0.64 mmol), 2-bromo-1-(4-methoxyphenyl)ethanone (160 mg, 0.69 mmol) and potassium carbonate (132 mg, 0.95 mmol) in N,N-dimethylformamide (4 mL) was stirred at room temperature overnight. At this time, the light brown reaction mixture was quenched with water. The resulting precipitate was collected by filtration and dried in vacuo. The resulting solid was dissolved in methylene chloride, concentrated in vacuo and then triturated with diethyl ether. The resulting solid was collected by filtration and dried in vacuo to afford 5-bromo-1-[2-(4-methoxy-phenyl)-2-oxo-ethyl]-1H-pyrrole-2-carboxylic acid methyl ester (155 mg, 69%) as light brown solid. 1H NMR (chloroform-d) δ ppm 8.00 (d, J=8.8 Hz, 2H), 6.96-7.07 (m, 3H), 6.85 (d, J=1.8 Hz, 1H), 5.71 (s, 2H), 3.91 (s, 3H), 3.75 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841299B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-835237f0d9e14a5ca87c545061af1202 |
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| Source note | uspto-grants-2014_09 |
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