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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 4-methyl-1h-pyrrole-3-carboxylateHCID 235044—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-bromo-4-methyl-1H-pyrrole-3-carboxylateHCID 6692511486%

Reaction Conditions

Temperature-30 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026237B2
Source datasetuspto-grants-2011_09
ORD IDord-75654bcaff424a289fca944869786fe7
Source noteuspto-grants-2011_09