HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Diethyl 2-(2-naphthyl)malonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Carbonate | HCID 7766 | — |
| Reactant | Ethyl 2-naphthylacetate | HCID 256821 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Product | Diethyl 2-(2-naphthyl)malonate | HCID 15668316 | — |
Reaction Steps
To a solution of ethyl 2-naphtylacetate (2 g) in 23.3 ml of diethylcarbonate, kept under stirring and at room temperature, are added portionwise 0.232 g of sodium. The reaction mixture is refluxed for 2 hours 30 minutes, then it is concentrated in order to eliminate the not reacted diethylcarbonate and it is added with 20 ml of cold water. The resulting mixture is acidified with acetic acid until weak acidity is reached, then it is extracted three times with diethyl ether. The pooled organic extracts are dried over sodium sulfate and the solvent is evaporated off, to give, after recrystallization from diethyl ether (19 ml), 1.015 g of the product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06472396B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-4ec4206765604ab9a956c17eb754fed5 |
| Source note | uspto-grants-2002_10 |