HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 1-[4-(4-Benzylpiperazin-1-yl)phenyl]ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Piperazin-4-ylacetophenone | HCID 97269 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-[4-(4-Benzylpiperazin-1-yl)phenyl]ethanone | HCID 757808 | 54.1% |
Reaction Steps
A mixture of 1-(4-piperazin-1-yl-phenyl)-ethanone (500 mg, 2.45 mmol), benzaldehyde (312 mg, 2.94 mmol) and NaBH(OAc)3 (778 mg, 3.67 mmol) in AcOEt (15 ml) was stirred at room temperature overnight. The resulting solution was partitioned between water and DCM and the organic phase was dried over Na2SO4 and evaporated in vacuo. The crude product was purified by silica gel chromatography (eluent: DCM/MeOH/NH4OH 95:5:0.2) to give 390 mg of 1-[4-(4-benzyl-piperazin-1-yl)-phenyl]-ethanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08242175B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-b8e8179a00464bc988c4bee90f5f1b3b |
| Source note | uspto-grants-2012_08 |