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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1962483Generated: 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/1962483

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 filtered, 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 filtered, 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 numberUS08415368B2
Source datasetuspto-grants-2013_04
ORD IDord-d2a981a3792a41eebc9f46a2cf895b27
Source noteuspto-grants-2013_04