HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 4-((2S)-1,4-dibenzylpiperazin-2-yl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | (2S)-1,4-dibenzyl-2-(4-bromophenyl)piperazine | HCID 66594629 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-((2S)-1,4-dibenzylpiperazin-2-yl)benzaldehyde | HCID 86634557 | 41% |
Reaction Steps
n-Butyllithium (1.56M in hexane, 14 ml, 21.8 mmol) was added to a solution of (2S)-1,4-dibenzyl-2-(4-bromophenyl)piperazine (6.1 g, 14.5 mmol) in tetrahydrofuran (60 ml) at −78° C. After one hour stirring, dimethylformamide (1.6 g, 21.9 mmol) was added and the solution was stirred for one hour. The mixture was partitioned between water and chloroform. The organic layer was washed with brine, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting 5-10% methanol in chloroform to furnish 4-((2S)-1,4-dibenzylpiperazin-2-yl)benzaldehyde (1.6 g, 41%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129377B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-e15847031e8e45eaa77ca1fcf6e68f9d |
| Source note | uspto-grants-2012_03 |