HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Iodophenol → 2-(4-Vinyl-phenyl)-benzo[b]furan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Iodophenol | HCID 10784 | — |
| Reactant | 1-Ethenyl-4-ethynylbenzene | HCID 10942441 | — |
| Product | 2-(4-Vinyl-phenyl)-benzo[b]furan | HCID 11252986 | — |
Reaction Steps
The general procedure was used to convert 1-Ethynyl-4-vinyl-benzene and 2-iodophenol to the title product. Purification by flash chromatography (hexanes as the eluent) gave the analytically pure product as a white solid (300 mg, 68% yield). 1H NMR (300 MHz, CDCl3) δ 7.79 (d, J=8.45, 2H), 7.56-7.44 (m, 4H), 7.29-7.19 (m, 2H), 6.98 (s, 1H), 6.74 (dd, J=10.93 and J=6.59, 1H), 5.78 (d, J=17.71, 1H), 5.28 (d, J=10.93, 1H). 13C NMR (75 MHz, CDCl3) δ 155.66, 154.87, 137.69, 136.26, 129.75, 129.22, 126.61, 125.02, 124.28, 122.94, 120.87, 114.40, 111.13, 101.37. Anal. Calcd. for C16H12O: C, 87.25; H, 5.49. Found C, 87.54; H, 5.62. m.p.: 164-165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07473786B1 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-71c2bbbea578426c85cfc28e31af0b06 |
| Source note | uspto-grants-2009_01 |