HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → HCID 86612631, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | 2-Cyclohexen-1-one | HCID 13594 | — |
| Reactant | 2-Chloro-5-(4-methoxyphenyl)pyridine-3-carbaldehyde | HCID 15459226 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86612631 | HCID 86612631 | 91% |
Reaction Steps
The clear solution of 2-Chloro-5-(4-methoxyphenyl)-nicotinaldehyde (10 mmol, 2.45 g) and imidazole (10 mmol) in 50 ml. of MeOH was slowly charged with 50 ml. of deionized water. To a stirred homogeneous reaction mixture was added 2-cyclohexen-1-one (10.2 mmol., 1.0 g) at room temperature and reaction progress was monitored by TLC. Upon completion of the reaction, excess MeOH was removed under reduced pressure, washed with water and extracted with CHCl3 thrice. Combined organic layers were washed with brine solution twice. The organic layer was concentrated and column chromatography of the crude product on silica gel, using 30% EtOAc in hexane as eluent, gave pure Baylis-Hillman adduct in 91% yield (3.13 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07666883B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-b96204621b934505ab25d25350c51f79 |
| Source note | uspto-grants-2010_02 |