HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Iodotoluene → 2,3-Dimethoxy-5-[(2-methylphenyl)ethynyl]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Iodotoluene | HCID 5128 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 5-Ethynyl-2,3-dimethoxypyridine | HCID 58213389 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2,3-Dimethoxy-5-[(2-methylphenyl)ethynyl]pyridine | HCID 71186209 | 56% |
Reaction Steps
Bis(triphenylphosphine)palladium(II) dichloride (50 mg, 0.07 mmol), copper (I) iodide (25 mg, 0.13 mmol) and 5-ethynyl-2,3-dimethoxypyridine (Intermediate 32) (500 mg, 3.1 mmol) were suspended in degassed triethylamine (5 ml) and dichloromethane (5 ml) to give a brown suspension. To this was added 1-iodo-2-methylbenzene (670 mg, 3.1 mmol) by syringe and the reaction was allowed to stir for 16 hours before being diluted with ethyl acetate and washed with brine. The crude material was purified by column chromatography (SiO2; 0-10% ethyl acetate in petrol) to afford 2,3-dimethoxy-5-[(2-methylphenyl)ethynyl]pyridine (437 mg, 56% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09180122B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-a8ad6790e9884a6594565c890f2fe48a |
| Source note | uspto-grants-2015_11 |