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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451362Generated: October 30, 2026

Sodium Carbonate → methyl 5-[4-chloro-2-(trifluoromethyl)phenyl]-4-methyl-1H-pyrrole-3-carboxylate

https://huagongshe.com/reaction/451362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Chloro-2-(trifluoromethyl)phenylboronic AcidHCID 2763244—
ReactantMethyl 5-bromo-4-methyl-1H-pyrrole-3-carboxylateHCID 66924763—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventEthyl AcetateHCID 8857—
SolventToluene waterHCID 22272177—
Productmethyl 5-[4-chloro-2-(trifluoromethyl)phenyl]-4-methyl-1H-pyrrole-3-carboxylateHCID 5848851465%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of methyl 5-bromo-4-methyl-1H-pyrrole-3-carboxylate (0.44 g, 2.0 mmol), [4-chloro-2-(trifluoromethyl)phenyl]boronic acid (0.90 g, 4.0 mmol), Na2CO3 (0.64 g, 6.0 mmol) and palladium tetrakis(triphenylphosphine) (0.12 g, 0.10 mmol) in toluene/water (9:1, 10 ml) was stirred at 110° C. for 2.0 h under N2. The reaction mixture was cooled to room temperature and diluted with ethyl acetate. The mixture was washed with water and brine, then dried over sodium sulfate and concentrated on a rotary evaporator. The resulting residue was purified by silica-gel column chromatography (dichloromethane) to give the title compound (0.41 g, 65%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487117B2
Source datasetuspto-grants-2013_07
ORD IDord-72fefe348b6a43c5bc1fcddcf9400c17
Source noteuspto-grants-2013_07