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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420692Generated: October 31, 2026

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

https://huagongshe.com/reaction/2420692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium CarbonateHCID 10340—
Reactant4-Chlorophenylboronic acidHCID 74299—
ReactantMethyl 4-bromo-1H-pyrrole-2-carboxylateHCID 2763594—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Productmethyl 4-(4-chlorophenyl)-1H-pyrrole-2-carboxylateHCID 6721553325%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a stirred DMF solution (40 mL) containing methyl 4-bromo-1H-pyrrole-2-carboxylate (1.0 g, 4.9 mmol), commercially available from Bionet, and Pd(Ph3)4 (195 mg, 0.17 mmol) was added Na2CO3 (1.3 g, 12.52 mmol) (dissolved in minimum amount water) and 4-chlorophenyl boronic acid (0.85 g, 5.43 mmol) under Ar. The mixture was degassed, with Ar prior to stirring overnight at 110° C. After cooling the reaction to RT, it was diluted with 10 mL of water and 200 mL of EtOAc. The aqueous layer was extracted, with EtOAc (3×20 mL). The organic layers were combined, dried over Na2SO4, and cone, in vacuo to yield a brown oil. The oil was purified by column chromatography (silica gel, 0%-15% gradient elution with EtOAc/hexanes) to yield 288 mg (25%) of product as white solid. MS (ESI) 236 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956049B2
Source datasetuspto-grants-2011_06
ORD IDord-df68e304a4aa45ad842f53808298ae6c
Source noteuspto-grants-2011_06