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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912586Generated: October 25, 2026

Bromine → ethyl 4-bromo-3,5-dimethyl-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/912586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant1H-Pyrrole-2-carboxylic acid, 3,5-dimethyl-, ethyl esterHCID 137477—
SolventCarbon TetrachlorideHCID 5943—
SolventDichloromethaneHCID 6344—
Productethyl 4-bromo-3,5-dimethyl-1H-pyrrole-2-carboxylateHCID 138486—

Reaction Steps

To a solution of ethyl 3,5-dimethyl-1H-pyrrole-2-carboxylate (3.42 g, 20 mmol) in carbon tetrachloride (40 mL) was added a solution of bromine in carbon tetrachloride (10 mL) dropwise at 20° C. After the addition was complete, stirring was continued for 2 h. The reaction mixture was diluted with DCM, washed with aqueous NaHCO3 and water, and then dried over Na2SO4. Evaporation of solvent gave ethyl 4-bromo-3,5-dimethyl-1H-pyrrole-2-carboxylate as a solid (4.8 g), which was used in the next step without purification. 1H-NMR (CDCl3): δ 9.36 (1H, s), 4.30 (2H, q), 2.28 (3H, s), 2.26 (3H, s), 1.36 (3H, t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026237B2
Source datasetuspto-grants-2011_09
ORD IDord-c42fdd84f13e4bc9a801ccb67316cb09
Source noteuspto-grants-2011_09