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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070367Generated: October 29, 2026

methyl 2-chloro-5-(2-fluorophenyl)-4-methyl-1H-pyrrole-3-carboxylate → Methyl 5-(2-fluorophenyl)-4-methyl-1H-pyrrole-3-carboxylate

https://huagongshe.com/reaction/2070367

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 2-chloro-5-(2-fluorophenyl)-4-methyl-1H-pyrrole-3-carboxylateHCID 66924695—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductMethyl 5-(2-fluorophenyl)-4-methyl-1H-pyrrole-3-carboxylateHCID 6692428076%

Reaction Steps

To a solution of methyl 2-chloro-5-(2-fluorophenyl)-4-methyl-1H-pyrrole-3-carboxylate (10.2 g) in methanol (200 mL) was added 10% palladium carbon (50% containing water, 1.28 g), and the mixture was stirred under a hydrogen atmosphere at room temperature for 20 hr. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. A saturated aqueous sodium hydrogencarbonate solution (100 mL) was added to the residue, 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, filtered, and concentrated under reduced pressure. Recrystallization of the residue from ethyl acetate-hexane gave the title compound as white crystals (yield 6.70 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299261B2
Source datasetuspto-grants-2012_10
ORD IDord-a4bf81a696ae4f30a6741154aa83f169
Source noteuspto-grants-2012_10