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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909887Generated: November 1, 2026

Dimethylformamide → methyl 1-(4-chlorobenzyl)-4-phenyl-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/1909887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium CarbonateHCID 10340—
ReactantPhenyl dihydrogen orthoborateHCID 78412—
Reactantmethyl 4-bromo-1-(4-chlorobenzyl)-1H-pyrrole-2-carboxylateHCID 58306731—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Productmethyl 1-(4-chlorobenzyl)-4-phenyl-1H-pyrrole-2-carboxylateHCID 5830676736.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of methyl 4-bromo-1-(4-chlorobenzyl)-1H-pyrrole-2-carboxylate (0.72 g) and DMF (21 mL) were added phenylboric acid (0.30 g), sodium carbonate (0.58 g), water (3.0 mL), and tetrakis(triphenylphosphine) palladium (0.13 g), followed by stirring at 100° C. for 24 hours. To the reaction mixture were added ethyl acetate and water, and the insoluble materials were separated by filtration through Celite. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and then filtered. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=0 to 10%) to obtain methyl 1-(4-chlorobenzyl)-4-phenyl-1H-pyrrole-2-carboxylate (0.26 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598355B2
Source datasetuspto-grants-2013_12
ORD IDord-41c9e67cb03f47c0b0d706c6b2563bd7
Source noteuspto-grants-2013_12