HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl methylmalonate → Diethyl (3-oxo quinuclidin-2-yl)methyl-methylmalonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl methylmalonate | HCID 11857 | — |
| Reactant | 2-Methylene-3-quinuclidone | HCID 322973 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Diethyl (3-oxo quinuclidin-2-yl)methyl-methylmalonate | HCID 54084773 | — |
Reaction Steps
Ethanolic sodium ethoxide, previously prepared from 2.9 g of metallic sodium and 100 ml of ethanol, was added to diethyl methyl-malonate, 50 g, and the mixture was refluxed for 30 min. then cooled to 5°. A solution of 2-methylenequinuclidin-3-one, 39.4 g, in ethanol, 50 ml, was then added dropwise and with stirring. After 16 hrs. at room temperature, the resulting solution was neutralized with acetic acid then subjected to evaporation at reduced pressure. Water, 100 ml was added and the mixture was extracted with chloroform. Evaporation of this solvent gave diethyl (3-oxo quinuclidin-2-yl)-methyl-methylmalonate, 72 g (81%), m.p., 58.4° (from petroleum ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04309544 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-bb1ae86741a34ec0b8f989f63622ce57 |
| Source note | uspto-grants-1982_01 |