HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(4-(4-(Phenylmethyl)-1-piperazinyl)phenyl)acetamide → N-[4-(1-Piperazinyl)phenyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(4-(4-(Phenylmethyl)-1-piperazinyl)phenyl)acetamide | HCID 960610 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-[4-(1-Piperazinyl)phenyl]acetamide | HCID 15631761 | 56% |
Reaction Steps
This compound was prepared by the hydrogenation of 7.7 (0.025 mole) of N-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]acetamide in 100 ml of methanol using palladium on carbon as the catalyst. The solution was filtered and the filtrate concentrated under reduced pressure to give an oil which crystallized. The solid was dissolved in a minimum amount of a methylene chloride/10% methanol solution and passed through a 100 g Florisil® column. The desired fractions were concentrated to an oil under reduced pressure which crystallized to give 3.1 g (56%) crude product. A 0.5 g portion was recrystallized from methanol/petroleum ether to give cream colored solid, m.p. 191°-193° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04960776 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-fea3129dcd2645d18642fb590b795be2 |
| Source note | uspto-grants-1990_10 |