HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium amide → 2,6-Diethyl-2,3,6-trimethyl-4-piperidyl p-t-butylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium amide | HCID 24532 | — |
| Reactant | Methyl p-tert-butylbenzoate | HCID 97433 | — |
| Reactant | 2,6-Diethyl-2,3,6-trimethylpiperidin-4-ol | HCID 22182241 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 2,6-Diethyl-2,3,6-trimethyl-4-piperidyl p-t-butylbenzoate | HCID 21330294 | 104.2% |
Reaction Steps
15.0 g of 2,6-diethyl-2,3,6-trimethyl-4-piperidinol (Compound 1) and 16.0 g of methyl p-t-butylbenzoate were dissolved in 500 ml of heptane. 1.5 g of lithium amide were then added to the solution and the mixture was refluxed by heating in a flask equipped with a Dean-Stark separator. 1.5 g of methanol were first removed and this was followed by 200 ml of heptane, which distilled off over a period of 3 hours. After cooling the reaction mixture, it was washed with water and dried over magnesium sulphate; the solvent was then removed by evaporation under reduced pressure. The residue was distilled under reduced pressure, giving 28.2 g of the title compound as a colourless liquid (bp 176°-178° C./0.008 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04141883 |
| Source dataset | uspto-grants-1979_02 |
| ORD ID | ord-b1322756b7e547ee99e2b1fba4888fb3 |
| Source note | uspto-grants-1979_02 |