HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Cyclopropyl-7-iodo-5-nitrobenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2,6-Diiodo-4-nitrophenol | HCID 9370 | — |
| Reactant | Cyclopropylacetylene | HCID 138823 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Cyclopropyl-7-iodo-5-nitrobenzofuran | HCID 118021828 | 78.3% |
Reaction Steps
A solution of 2,6-diiodo-4-nitrophenol (10 g, 25.6 mmol), ethynylcyclopropane (1.9 g, 28.8 mmol) and Cu2O (1.9 mg, 13.2 mmol) in 100 mL of dry pyridine was refluxed for 2 h. The reaction mixture was poured into 1 L of water and stirred for 10 min. The resulting mixture was filtered. The cake was purified by column chromatography on silica gel eluting with EtOAc/PE (0-20%) to give the title compound (6.6 g, 78% yield) as a yellow solid. 1H NMR (CDCl3, 400 MHz): δ 8.47 (d, J=2.4 Hz, 1H), 8.32 (d, J=2.4 Hz, 1H), 6.58 (s, 1H), 2.13-2.07 (m, 1H), 1.14-1.04 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09034900B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-4b2f26ebe7c04741a0075a3e848b80ba |
| Source note | uspto-grants-2015_05 |