HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Ethylcyclopentane-1,3-dione → 2-Ethyl-2-(6-m-methoxyphenyl-5-methyl-3-oxohexyl)cyclopentane-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Ethylcyclopentane-1,3-dione | HCID 69978 | — |
| Reactant | 1-Diethylamino-6-(m-methoxyphenyl)-5-methylhexan-3-one | HCID 21485407 | — |
| Reactant | 5-Methyl-6-(m-methoxyphenyl)hex-1-en-3-one | HCID 21485478 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 2-Ethyl-2-(6-m-methoxyphenyl-5-methyl-3-oxohexyl)cyclopentane-1,3-dione | HCID 21485626 | — |
Reaction Steps
Add a mixture of 1-diethylamino-6-(m-methoxyphenyl)-5-methylhexan-3-one and 5-methyl-6-(m-methoxyphenyl)hex-1-en-3-one (6 g, prepared by slow distillation of the former substance) to 2-ethylcyclopentane-1,3-dione (3.5 g) in 0.12% methanolic potassium hydroxide (10 cc) and heat the mixture under reflux for 6 hours. Remove most of the solvent under reduced pressure and add ether (25 cc) and benzene (25 cc) to the residue. Wash the solution with 5% aqueous sodium hydroxide, water, dilute hydrochloric acid, and brine, and dry. Evaporate the solvent to obtain a viscous brown gum, which is the triketone 2-ethyl-2-(6-m-methoxyphenyl-5-methyl-3-oxohexyl)cyclopentane-1,3-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03959322 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-7a35113cc7024972af5d9d45f8589e0a |
| Source note | uspto-grants-1976_05 |