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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886936Generated: November 1, 2026

Ethyl Acetate → Benzoxazole, 5-nitro-2-(2-thienyl)-

https://huagongshe.com/reaction/1886936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2-(Tri-n-butylstannyl)thiopheneHCID 2779373—
Reactant2-Chloro-5-nitrobenzo[d]oxazoleHCID 10352723—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductBenzoxazole, 5-nitro-2-(2-thienyl)-HCID 112536212%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-chloro-5-nitrobenzo[d]oxazole (404 mg, 2.04 mmol), 2-(tributylstannyl)-thiophene (648 μL, 2.04 mmol) and tetrakis(triphenylphosphine)palladium (0) (40.8 mg) in dioxane (12.2 mL) was heated at 100° C. for 16 h under nitrogen. Ethyl acetate was added, the organic layer was washed with water, dried over anhydrous MgSO4 and evaporated. The resulting solid was purified by column chromatography eluting with ethyl acetate/hexanes 10:90 v/v, and then purified by reverse phase HPLC to afford 3 mg (2%) of the title product (LCMS RT=6.95 min)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501713B2
Source datasetuspto-grants-2013_08
ORD IDord-d29bb355965948ef8e107ae20d272ecc
Source noteuspto-grants-2013_08