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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012389Generated: October 30, 2026

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

https://huagongshe.com/reaction/1012389

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 numberUS07977488B2
Source datasetuspto-grants-2011_07
ORD IDord-73ba155e800f4dd8b418ff3faae2fa22
Source noteuspto-grants-2011_07