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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178113Generated: October 27, 2026

Sodium Carbonate → Ethyl 5-phenyl-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/1178113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
Reactantethyl 5-bromo-1H-pyrrole-2-carboxylateHCID 59559613—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventToluene waterHCID 22272177—
ProductEthyl 5-phenyl-1H-pyrrole-2-carboxylateHCID 1237803367.95%

Reaction Steps

Na2CO3 (97.5 mg, 0.92 mmol) was added to a stirred solution of 5-bromo-1H-pyrrole-2-carboxylic acid ethyl ester (100 mg, 0.46 mmol) in toluene: H2O (5:1, 11 mL). Pd (PPh3)4 (53 mg, 0.046 mmol) and phenylboronic acid (84.3 mg, 0.7 mmol) were then added and the reaction mixture was heated to reflux for 2 hrs. The reaction mixture was then diluted with water and the product was extracted with ethyl acetate. The organic layer was washed with saturated brine solution, dried over sodium sulphate and concentrated to get the residue. The residue obtained was purified by column chromatography (using silica gel of 60-120 mesh and 5% EtOAc in Hexane as eluent) afford 67 mg (67.95% yield) of 5-phenyl-1H-pyrrole-2-carboxylic acid ethyl ester. 1H NMR (CDCl3): δ 9.4 (s, 1H), 7.64 (d, 2H), 7.48 (t, 2H), 7.36 (d, 11H), 7.0 (s, 1H), 6.58 (s, 1H), 4.4 (q, 2H), 1.4 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-18352064f7724b60867a5fb68417d3d0
Source noteuspto-grants-2010_11