HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673288Generated: October 31, 2026
4-Iodo-2-methylphenol → HCID 67341414, compound
https://huagongshe.com/reaction/1673288
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Iodo-2-methylphenol | HCID 143713 | — |
| Reactant | HCID 86622032 | HCID 86622032 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67341414 | HCID 67341414 | 61.3% |
Reaction Steps
To a solution of 4-ethynyl-3-(2,3,4,6-tetra-O-pivaloyl-β-D-glucopyranosyloxy)-1H-indazole (66 mg) in triethylamine (1 mL) were added 4-iodo-2-methylphenol (25 mg), tetrakis(triphenylphosphine)palladium (0) (12 mg) and copper (I) iodide (4 mg), and the mixture was stirred at 80° C. under an argon atmosphere overnight. The reaction mixture was cooled to room temperature and diluted with ethyl acetate. The insoluble material was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: n-hexane/ethylacetate=3/1-2/1-1/1) to give the title compound (47 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07998975B2 |
|---|
| Source dataset | uspto-grants-2011_08 |
|---|
| ORD ID | ord-cb39498241c54576807e93b30f9b2028 |
|---|
| Source note | uspto-grants-2011_08 |
|---|