HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Methyl-6-{3-[4-(2-methoxyphenyl)-1-piperazinyl]-2-methyl-1-propenyl}benzoxazolinone → 3-Methyl-6-{3-[4-(2-methoxyphenyl)-1-piperazinyl]-2-methylpropyl}benzoxazolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Methyl-6-{3-[4-(2-methoxyphenyl)-1-piperazinyl]-2-methyl-1-propenyl}benzoxazolinone | HCID 53932079 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Methyl-6-{3-[4-(2-methoxyphenyl)-1-piperazinyl]-2-methylpropyl}benzoxazolinone | HCID 14556353 | — |
Reaction Steps
0.01 mole of 3-methyl-6-{3-[4-(2-methoxyphenyl)-1-piperazinyl]-2-methyl-1-propenyl}benzoxazolinone is dissolved in absolute ethanol in a 500-cm3 flask equipped with a three-way tap and a magnetic stirrer. 0.5 g of Raney nickel is added and the mixture is stirred under a hydrogen atmosphere at room temperature and atmospheric pressure. After the theoretical amount of hydrogen has been absorbed, the reaction medium is filtered, the filtrate is evaporated to dryness on a water bath under vacuum and the residue is recrystallized in cyclohexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04960778 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-b3dbd893b9f54718a709a03d120ce841 |
| Source note | uspto-grants-1990_10 |