HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-Bromo-2-(4-methoxyphenyl)benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Ethynyl-4-methoxybenzene | HCID 251020 | — |
| Reactant | 4-Bromo-2-iodophenol | HCID 10924532 | — |
| Solvent | DMF Diethylamine | HCID 86589549 | — |
| Product | 5-Bromo-2-(4-methoxyphenyl)benzofuran | HCID 10149571 | 45% |
Reaction Steps
A solution of 4-Bromo-2-iodophenol [207115-22-8] (0.9 g, 3.0 mmol), 4-Methoxyphenylacetylene (0.43 g, 3.3 mmol), PdCl2P(PH3)2 (70 mg), and Cul (50 mg) in DMF/Diethylamine (10 ml) was heated to 60° C. After 1 hr, the reaction was cooled and poured into water which was extracted with EtOAc. The organic layer was dried over MgSO4 and concentrated to give a solid which was triturated with MeOH, filtered to give a solid (0.4 g, 45%): Mp=192–194° C.; 1H NMR (CDCl3) δ 7.77 (d, 2 H, J=9.1 Hz), 7.66 (s, 1 H), 7.37–7.32 (m, 2 H), 6.98 (d, 2 H, J=9.1 Hz), 6.82 (d, 1 H, J=0.8 Hz), 3.87 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07022733B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-b13d49a720a0401589d953ba19e5bef2 |
| Source note | uspto-grants-2006_04 |