HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-m-Methoxyphenylhex-1-en-3-one → 2-Cetyl-2-(6-m-methoxyphenyl-3-oxohexyl)-1,3-cyclopentanedione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-m-Methoxyphenylhex-1-en-3-one | HCID 10798238 | — |
| Reactant | 2-Cetylcyclopentane-1,3-dione | HCID 13622428 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 2-Cetyl-2-(6-m-methoxyphenyl-3-oxohexyl)-1,3-cyclopentanedione | HCID 21485591 | 73.7% |
Reaction Steps
Reflux a mixture of 2-cetylcyclopentane-1,3-dione (10.1 g), 6-m-methoxyphenylhex-1-en-3-one (6.0 g) and 0.02% methanolic potassium hydroxide solution (120 cc) for 26 hours and then cool. Dissolve the residue obtained after removal of solvent under reduced pressure in a mixture of benzene (50 cc) and ether (50 cc), and wash the solution in turn with sodium carbonate solution, 10% aqueous sulfuric acid and water. Remove the solvent by evaporation under reduced pressure to obtain as residue crude 2-cetyl-2-(6-m-methoxyphenyl-3-oxohexyl)-1,3-cyclopentanedione (11.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04002746 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-20b444c2fcf446a1b4276ef0e7e5ec57 |
| Source note | uspto-grants-1977_01 |