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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247221Generated: October 31, 2026

Ethanol → 5-Methoxy-2-(4-methoxyphenyl)-7-phenyl-1,3-benzoxazole

https://huagongshe.com/reaction/1247221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
Reactant7-Bromo-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazoleHCID 12148969—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product5-Methoxy-2-(4-methoxyphenyl)-7-phenyl-1,3-benzoxazoleHCID 21907367—

Reaction Steps

7-Bromo-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazole (200 mg, 0.60 mmol) and tetrakis(triphenylphosphine)palladium(0) (63 mg, 0.03 mmol) were dissolved in toluene (5 mL) and stirred for 10 min at room temperature under a nitrogen atmosphere. Benzene boronic acid (110 mg, 0.90 mmol) was added, followed by aqueous sodium carbonate (2 M, 1.5 mL) and ethanol (2 mL). The mixture was refluxed for 12 h, diluted with water and extracted with EtOAc. The organic extracts were dried over MgSO4. Evaporation and purification by flash chromatography (20%–40% EtOAc/petroleum ether) gave the title compound as a light pink solid, mp 92° C.; MS m/e 332 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129258B2
Source datasetuspto-grants-2006_10
ORD IDord-5fab5b5e23fc4686acd1954b8a9a01f2
Source noteuspto-grants-2006_10