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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930327Generated: November 2, 2026

Pyridine → Ethyl 3-(1,1-dimethylethyl)-1-(3-fluorophenyl)-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/1930327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3-Fluorophenylboronic acidHCID 2733986—
ReactantEthyl 3-tert-butyl-1H-pyrazole-5-carboxylateHCID 2743509—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-(1,1-dimethylethyl)-1-(3-fluorophenyl)-1H-pyrazole-5-carboxylateHCID 6904245554.1%

Reaction Steps

3-Fluorophenylboronic acid (0.70 g, 5.0 mmol), ethyl 3-tert-butyl-1H-pyrazole-5-carboxylate (0.981 g, 5.0 mmol), Cu(OAc)2 (0.908 g, 5.0 mmol), pyridine (2.45 ml, 30 mmol) and 4A MS (1.9 g) were combined in CH2Cl2 (48 ml) and stirred open to air at RT for 4 d. The reaction mixture was diluted with EtOAc (150 mL), washed with 3M HCl (2×50 mL), H2O (50 mL) and brine (50 mL), dried (MgSO4) and concentrated in vacuo. The crude product was purified by chromatography to afford ethyl 3-tert-butyl-1-(3-fluorophenyl)-1H-pyrazole-5-carboxylate (0.786 g, 54% yield) as colorless oil. MS (ESI) m/z: 291 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188113B2
Source datasetuspto-grants-2012_05
ORD IDord-937a4cb5c5614dcf843e94eae86e6ddd
Source noteuspto-grants-2012_05