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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383754Generated: October 30, 2026

Sodium Carbonate → 1,4-dimethyl-5-(4-fluorophenyl)-1H-pyrrole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/383754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Fluorophenylboronic acidHCID 285645—
Reactantethyl 5-bromo-1,4-dimethyl-1H-pyrrole-3-carboxylateHCID 59808055—
CatalystHCID 178418397HCID 178418397—
SolventDichloromethaneHCID 6344—
SolventN,N-Dimethylformamide--water (1/1)HCID 21962138—
Product1,4-dimethyl-5-(4-fluorophenyl)-1H-pyrrole-3-carboxylic acid ethyl esterHCID 6725316296.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of ethyl 5-bromo-1,4-dimethyl-1H-pyrrole-3-carboxylate (246 mg, 1.0 mmol), 4-fluorophenyl-boronic acid (210 mg, 1.5 mmol), Na2CO3 (320 mg, 3.0 mmol) and Pd(PPh3)4 (116 mg, 0.10 mmol) in DMF/H2O (10:1, 10 mL) was sparged with nitrogen for 10 min. The reaction vial was sealed and heated at 110° C. with stirring. After 18 h, the reaction mixture was diluted with DCM and then filtered. The filtrate was concentrated under reduced pressure and then purified by column chromatography, eluting with EtOAc-Hex (0:100 to 50:50), to give 1,4-dimethyl-5-(4-fluorophenyl)-1H-pyrrole-3-carboxylic acid ethyl ester (252 mg, 96%) as a pale yellow solid. 1H-NMR (CDCl3): δ 7.30 (1H, s), 7.26-7.20 (2H, m), 7.15-7.10 (2H, m), 4.28 (2H, q), 3.48 (3H, s), 2.20 (3H, s), 1.36 (3H, t). MS (ESI): 262 (MH+). The title compound was prepared from 1,4-dimethyl-5-(4-fluorophenyl)-1H-pyrrole-3-carboxylic acid ethyl ester in a manner similar to that described for Examples 16C-D.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367667B2
Source datasetuspto-grants-2013_02
ORD IDord-4342a3d616584d9dba635ebd52539806
Source noteuspto-grants-2013_02