HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611937Generated: November 1, 2026
Tris(furan-2-yl)phosphane → [7-(3,6-dihydro-2H-pyran-4-yl)-4-methoxy-benzooxazol-2-yl]-carbamic acid methyl ester
https://huagongshe.com/reaction/1611937
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tris(furan-2-yl)phosphane | HCID 521585 | — |
| Reactant | 4-Tributylstannyl-3,6-dihydro-2H-pyran | HCID 22252258 | — |
| Reactant | (7-Iodo-4-methoxy-benzooxazol-2-yl)-carbamic acid methyl ester | HCID 23593642 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | [7-(3,6-dihydro-2H-pyran-4-yl)-4-methoxy-benzooxazol-2-yl]-carbamic acid methyl ester | HCID 23593641 | 42.3% |
Reaction Steps
To a stirred solution of 350 g (10.1 mmol) (7-iodo-4-methoxy-benzooxazol-2-yl)-carbamic acid methyl ester in 50 ml dioxane were added 5.63 g (15.1 mmol) tributyl-(3,6-dihydro-2H-pyran-4-yl)-stannane, 173 mg (0.30 mmol) bis(dibenzylideneacetone)palladium(0), 374 mg (1.61 mmol) tri(2-furyl)phospine. The mixture was heated at 100° C. for 22 h and then poured onto water and extracted three times with ethyl acetate. The combined organic phases were dried over sodium sulfate and concentrated in vacuo. Flash chromatography (2/98 methanol/dichloromethane then 5/95 methanol/dichloromethane) followed by trituration in dichloromethane afforded 1.30 g (42%) [7-(3,6-dihydro-2H-pyran-4-yl)-4-methoxy-benzooxazol-2-yl]-carbamic acid methyl ester as a white solid. ES-MS m/e (%): 305 (M+H+, 100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06992083B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-faebdaf524424a6ca0ef2b187b7fb512 |
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| Source note | uspto-grants-2006_01 |
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