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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858257Generated: October 31, 2026

2-(Tributylstannyl)furan → 7-(2-Furyl)-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazole

https://huagongshe.com/reaction/858257

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)furanHCID 4393688—
Reactant7-Bromo-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazoleHCID 12148969—
CatalystHCID 178424406HCID 178424406—
SolventP-XyleneHCID 7809—
SolventAmmonium ChlorideHCID 25517—
Product7-(2-Furyl)-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazoleHCID 2190739299%

Reaction Steps

7-Bromo-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazole (300 mg, 0.90 mmol) and dichlorobis(tri-o-tolylphosphine)palladium(II) (71 mg, 0.09 mmol) were dissolved in p-xylene (3 mL) and stirred for 10 min at room temperature under a nitrogen atmosphere. 2-(Tributylstannyl)furan (449 mg, 1.26 mmol) was added and the mixture was refluxed for 4 hours. The mixture was cooled to room temperature, diluted with a saturated solution of ammonium chloride and extracted with EtOAc. The organic extracts were washed with water, then brine and dried over MgSO4 and concentrated. Purification by flash chromatography (20%–30% EtOAc/petroleum ether) gave the title compound as a white solid (99% yield, m.p. 120–121° C.); MS m/e 322 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148247B2
Source datasetuspto-grants-2006_12
ORD IDord-068bc544a42e471b95da15e2fde95822
Source noteuspto-grants-2006_12