HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-Iodophenyl)oxazole → 2-[4-[(4-Methoxyphenyl)methyl]phenyl]oxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-Iodophenyl)oxazole | HCID 9860258 | — |
| Reactant | HCID 178490612 | HCID 178490612 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[4-[(4-Methoxyphenyl)methyl]phenyl]oxazole | HCID 68488949 | 81.5% |
Reaction Steps
A Schlenk Flask was charged with tetrakis(triphenylphosphine)palladium(0) (0.42 g, 0.37 mmol), nitrogen, THF (20 ML), 2-(4-iodophenyl)oxazole (1 g, 3.7 mmol), and 4-methoxybenzyl zinc chloride (0.5 M in THF, 9.6 mL, 4.8 mmol). After 3 hours, the filtrate was concentrated. The resulting solid was treated with a mixture of ethyl acetate and a dilute aqueous ammonium chloride solution. The mixture was filtered and the organic layer was dried and concentrated. Purification on silica gel using a gradient of dichloromethane in hexane gave 0.8 g of 2-[4-[(4-methoxyphenyl)methyl]phenyl]oxazole, 1H NMR (400 MHz, CDCl3) δ 7.97 (d, 2H), 7.68 (s, 1H), 7.27 (d, 2H), 7.22 (s, 1H), 7.13 (d, 2H), 6.82 (d, 2H), 3.96 (s, 2H), 3.78 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737145B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-8e049b8b96ed452eac66c484c763dd3d |
| Source note | uspto-grants-2010_06 |