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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007356Generated: October 28, 2026

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

https://huagongshe.com/reaction/1007356

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 numberUS06794403B2
Source datasetuspto-grants-2004_09
ORD IDord-3c92cf56e8274c77973e9c1514a2be34
Source noteuspto-grants-2004_09