HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl methylmalonate → HCID 19909285, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl methylmalonate | HCID 11857 | — |
| Reactant | 1-Acetylcyclohexene | HCID 13612 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19909285 | HCID 19909285 | — |
Reaction Steps
Sodium metal (2.31 g, 101.0 mmol) is dissolved in 50 ml of ethanol, and diethyl methylmalonate (17.6 g, 101.0 mmol) is added, after which the mixture is stirred for approx. 30 min. under reflux. 1-Acetyl-1-cyclohexene (12.50 g, 101.0 mmol) is added and the mixture is stirred under reflux overnight. Potassium hydroxide (12.47 g, 222.2 mmol) dissolved in 40 ml of water is added and the mixture is heated under reflux for 4 hr. The ethanol is removed by rotary evaporation, and the residue is dissolved in water and washed with ether. The aqueous layer is acidified with conc. HCl and extracted with ether. The combined extracts are dried and the solvent is removed to give 4a,5,6,7,8,8a -hexahydro-4-methylnaphthalene-1,3(2H,4H)-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04921526 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-395828b73e014c2a8a7934969db5ff8e |
| Source note | uspto-grants-1990_05 |