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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419561Generated: October 29, 2026

Water → HCID 59452704, compound

https://huagongshe.com/reaction/419561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant(Pyridin-4-yl)boronic acidHCID 2734379—
Reactant4-Bromo-2-ethoxy-1-nitrobenzeneHCID 15555501—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventAcetic AcidHCID 176—
SolventDimethylacetamideHCID 31374—
ProductHCID 59452704HCID 5945270477.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 5-bromo-2-nitrophenyl ethyl ether (4.64 g, 18.86 mmol), PdCl2(dppf)*DCM (0.69 g, 0.94 mmol) and 4-pyridylboronic acid (4.03 g, 32.8 mmol) in N,N-dimethylacetamide (113 mL) was deoxygenated by bubbling with N2 (g) for ca 15 min. To this solution was added degassed 1.6 N K2CO3 (aq) (56.6 mL, 6.0 equiv.) and the resulting slurry was warmed to 80° C. for 24 h. The mixture was poured into 300 mL of H2O and neutralized with HOAc. The product was extracted with DCM, and dried (MgSO4). The solvent was rotovaped down and the crude product was purified by flash chromatography to give the title compound of step B (3.57 g, 14.62 mmol, 77.5%). 1H NMR (400 MHz, DMSO-d6) δ ppm 8.66-8.70 (m, 2H), 7.97 (d, J=8.42 Hz, 1H), 7.77-7.81 (m, 2H), 7.64 (d, J=1.65 Hz, 1H), 7.47 (dd, J=8.42, 1.65 Hz, 1H), 4.33 (q, J=6.96 Hz, 2H), 1.34 (t, J=6.96 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-732832f92ba34dd69d404a00226793d6
Source noteuspto-grants-2012_01