HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912582Generated: October 26, 2026
N-bromobutanimide → Ethyl 5-bromo-4-methyl-1H-pyrrole-3-carboxylate
https://huagongshe.com/reaction/912582
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl 4-methyl-1h-pyrrole-3-carboxylate | HCID 235044 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 5-bromo-4-methyl-1H-pyrrole-3-carboxylate | HCID 66925114 | 86% |
Reaction Steps
To a solution of ethyl 4-methyl-3-pyrrolecarboxylate (1.57 g, 10 mmol) in anhyd THF (30 mL) cooled to −78° C. was added NBS (1.9 g, 10 mmol). After stirring 1 h at −30° C., the reaction mixture was concentrated under reduced pressure. The residue was purified by column chromatography, eluting with EtOAc-Hex (0:100 to 30:70), to yield ethyl 5-bromo-4-methyl-1H-pyrrole-3-carboxylate (2.0, 86%) as a white solid. 1H-NMR (CDCl3): δ 8.54 (1H, brs), 7.38 (1H, d), 4.27 (2H, q), 2.24 (3H, s), 1.33 (3H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08026237B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-75654bcaff424a289fca944869786fe7 |
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| Source note | uspto-grants-2011_09 |
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