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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554214Generated: October 25, 2026

Ethyl 2-chloro-5-(2-fluorophenyl)-1H-pyrrole-3-carboxylate → Ethyl 5-(2-fluorophenyl)-1H-pyrrole-3-carboxylate

https://huagongshe.com/reaction/554214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-chloro-5-(2-fluorophenyl)-1H-pyrrole-3-carboxylateHCID 66924835—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductEthyl 5-(2-fluorophenyl)-1H-pyrrole-3-carboxylateHCID 6692469818.3%

Reaction Steps

To a solution (80 mL) of ethyl 2-chloro-5-(2-fluorophenyl)-1H-pyrrole-3-carboxylate (8.6 g) in ethanol was added 10% palladium carbon (50% containing water, 0.86 g), and the mixture was stirred under a hydrogen atmosphere at room temperature for 36 hr. The reaction mixture was filtrated, and the filtrate was concentrated under reduced pressure. The residue was dissolved in ethanol (70 mL), 10% palladium carbon (50% containing water, 0.90 g) was added, and the mixture was stirred under a hydrogen atmosphere at room temperature for 60 hr. The reaction mixture was filtrated, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=10:1→5:1) to give the title compound as a brown solid (yield 1.37 g, 18%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048909B2
Source datasetuspto-grants-2011_11
ORD IDord-1db86f55d7134dd3a2071c9533ea1506
Source noteuspto-grants-2011_11