HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → Benzyl 5-(4-methoxyphenyl)-6-methylpyridine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Iodo-3-(4-methoxyphenyl)-2-methylpyridine | HCID 57704805 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Benzyl 5-(4-methoxyphenyl)-6-methylpyridine-2-carboxylate | HCID 57704814 | — |
Reaction Steps
6-iodo-3-(4-methoxyphenyl)-2-methylpyridine (100 mg, 0.308 mmol), dichloro bis(triphenylphosphine)palladium(II) (22 mg, 0.031 mmol), triethylamine (46.7 mg, 0.462 mmol), benzyl alcohol (1 mL, 9.66 mmol) were mixed in acetonitrile (3 mL). The resulting mixture was placed under to carbon monoxide at 45 psi at 60° C. for 18 hours. The resulting reaction crude was purified by preparative TLC on SiO2 (eluted with 25% ethyl acetate in hexanes then 10% triethylamine, 20% ethyl acetate in hexanes) to afford benzyl 5-(4-methoxyphenyl)-6-methylpyridine-2-carboxylate. LCMS calc.=333.14; found=334.13 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915271B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-6c90803ebaa947b5b4e26d8fd12a9596 |
| Source note | uspto-grants-2011_03 |