Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1498935Generated: October 25, 2026

Sodium Hydroxide → Ethyl 4-bromopyrrole-2-carboxylate

https://huagongshe.com/reaction/1498935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantBromineHCID 24408—
ReactantEthyl 1H-pyrrole-2-carboxylateHCID 255670—
SolventCarbon TetrachlorideHCID 5943—
ProductEthyl 4-bromopyrrole-2-carboxylateHCID 532460738.2%

Reaction Steps

To a solution of ethyl 1H-pyrrole-2-carboxylate (1.17 g) in carbon tetrachloride (40 ml), a solution of bromine (1.48 g) in carbon tetrachloride (80 ml) was added dropwise at −15° C., and the mixture was stirred for one hour. The mixture was warmed to a room temperature, and a 2-N sodium hydroxide aqueous solution (80 ml) was added thereto. The resulting mixture was subjected to extraction with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate and concentrated under a reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:n-hexane=1:6) to give ethyl 4-bromo-1H-pyrrole-2-carboxylate (700 mg, 38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200008B2
Source datasetuspto-grants-2015_12
ORD IDord-7eb5723a9a564579ad270b68676c65d9
Source noteuspto-grants-2015_12