HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74484Generated: October 26, 2026
Ethanol → Ethyl 4-bromopyrrole-2-carboxylate
https://huagongshe.com/reaction/74484
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Ethyl 1H-pyrrole-2-carboxylate | HCID 255670 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Ethyl 4-bromopyrrole-2-carboxylate | HCID 5324607 | — |
Reaction Steps
1H-Pyrrole-2-carboxylic acid ethyl ester (10 g) was dissolved in carbon tetrachloride (50 ml). A carbon tetrachloride solution (50 ml) of bromine was added dropwise thereto on ice over 30 minutes. The reaction mixture was stirred at 25° C. for one hour. The suspension of reaction mixture was added dropwise to an ethanol solution (100 ml) of 10% sodium ethoxide on ice over 20 minutes. The solvent was concentrated under reduced pressure. The resulting residue was diluted with ethyl acetate (40 ml) and water (20 ml). The organic layer was washed with an aqueous solution saturated with sodium chloride (10 ml), and then concentrated. The residue obtained by concentration under reduced pressure was purified by silica gel column chromatography (hexane/ethyl acetate). Thus, a brown solid was obtained (10 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829199B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-fd68bc68f7e64f2d868a563444a0b180 |
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| Source note | uspto-grants-2014_09 |
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