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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Chlorophenylboronic acid | HCID 74299 | — |
| Reactant | Methyl 4-bromo-1H-pyrrole-2-carboxylate | HCID 2763594 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | methyl 4-(4-chlorophenyl)-1H-pyrrole-2-carboxylate | HCID 67215533 | 25% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07956049B2 |
|---|
| Source dataset | uspto-grants-2011_06 |
|---|
| ORD ID | ord-df68e304a4aa45ad842f53808298ae6c |
|---|
| Source note | uspto-grants-2011_06 |
|---|