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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090615Generated: November 1, 2026

Water → Methyl 5-bromo-1H-pyrrole-3-carboxylate

https://huagongshe.com/reaction/2090615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactantmethyl 1H-pyrrole-3-carboxylateHCID 12361759—
CatalystPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 5-bromo-1H-pyrrole-3-carboxylateHCID 2327115862%

Reaction Steps

A solution (30 mL) of methyl 1H-pyrrole-3-carboxylate (3.06 g) in tetrahydrofuran was cooled to −78° C., N-bromosuccinimide (4.38 g) and then pyridine (3 drops) were added, and the mixture was stirred at the same temperature for 1 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogencarbonate solution, water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=5:1) to give the title compound as a pale-yellow solid (yield 3.08 g, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436187B2
Source datasetuspto-grants-2013_05
ORD IDord-bf38d5054f2f4c86b35187c41cf40fa4
Source noteuspto-grants-2013_05