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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-(Tri-n-butylstannyl)thiophene | HCID 2779373 | — |
| Reactant | 2-Chloro-5-nitrobenzo[d]oxazole | HCID 10352723 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Benzoxazole, 5-nitro-2-(2-thienyl)- | HCID 11253621 | 2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501713B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-d29bb355965948ef8e107ae20d272ecc |
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| Source note | uspto-grants-2013_08 |
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