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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623735Generated: October 30, 2026

Potassium Phosphate, Dibasic → ethyl 3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/623735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, DibasicHCID 24450—
ReactantTrifluoromethanesulfonyl chlorideHCID 79000—
ReactantEthyl 3-(4-chlorophenyl)-1H-pyrrole-2-carboxylateHCID 79327547—
Catalystdichlorotris(1,10-phenanthroline)-ruthenium(II) hydrateHCID 16212249—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Productethyl 3-(4-chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-2-carboxylateHCID 86711826288.4%

Reaction Steps

This reaction was carried out in 5 batches using the same procedure. To a mixture of ethyl 3-(4-chlorophenyl)-1H-pyrrole-2-carboxylate [for synthesis see ACI-01] (1.25 g, 5.01 mmol), K2HPO4 (2.62 g, 15 mmol) and dichlortris(1,10-phenanthroline)-ruthenium(II) hydrate (71 mg, 0.10 mmol) in argon degassed dry MeCN (35 mL) was added CF3SO2Cl (1.60 mL, 15 mmol). The reaction mixture was stirred for 16 h at room temperature adjacent to a fluorescent light bulb (E27-32W, 4000K, 65 mA). After 16 h, an additional amount of CF3SO2Cl (0.20 mL, 1.88 mmol) was added and the reaction mixture was stirred overnight at room temperature adjacent to a fluorescent light bulb. All reaction mixtures were combined and diluted with EtOAc (150 mL) and H2O was added. The aqueous layer was extracted with EtOAc (150 mL). The organic layers were combined and the solvent was evaporated to give an oil. The crude product was purified by flash chromatography (silica, gradient heptane/EtOAc, 1:0→1:1) to furnish the desired product (4.59 g, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302988B2
Source datasetuspto-grants-2016_04
ORD IDord-592be9cc68064fd0961999e6f9fe138a
Source noteuspto-grants-2016_04