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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425603Generated: November 4, 2026

Toluene → HCID 136352338, compound

https://huagongshe.com/reaction/1425603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant2,5-Dibromo-3-nitropyridineHCID 298470—
Reactant4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 2734624—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
ProductHCID 136352338HCID 136352338—

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (300 mg, 1.36 mmol), 2,5-dibromo-3-nitropyridine (383 mg, 1.36 mmol), tetrakis(triphenylphosphine)palladium (31 mg, 0.027 mmol), Na2CO3 (4.3 mL, 2 M aqueous), 4.3 mL toluene, and 2.1 mL EtOH was vigorously stirred at 55° C. for 2 h. After cooling to rt, the volatiles were removed under reduced pressure and the residue was purified with silica chromatography (EtOAc in hexane, 5% to 35%) to afford 4-(5-bromo-3-nitropyridin-2-yl)phenol as a yellow wax (285 mg, 71%). MS (ESI) m/z [M+H]+295, 297.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08932557B2
Source datasetuspto-grants-2015_01
ORD IDord-acdb196889cd463d911b811c5d1793b0
Source noteuspto-grants-2015_01