HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 68691357, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Tert-butyl 4-(cyanomethyl)piperazine-1-carboxylate | HCID 21936030 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68691357 | HCID 68691357 | — |
Reaction Steps
To sodium hydride (0.1 g) taken in dry DMF (5 ml), under nitrogen, compound tert-butyl 4-(cyanomethyl)piperazine-1-carboxylate (0.5 g) was added and allowed to stir at room temperature for half an hour. Benzaldehyde (280 mg) was added to the above reaction mixture and allowed to stir for 3 hours at room temperature. The reaction mixture was quenched with ice water (50 ml) and extracted with ethyl acetate (3×10 ml). The combined organic layer was washed with brine (10 ml), dried over sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by column chromatography using MeOH: CH2Cl2 (0.5:9.5) as an eluent to afford tert-butyl 4-(1-cyano-2-phenylvinyl)piperazine-1-carboxylate as pure product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07807671B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-b0907b4d64b446efbd0194792cf4edbf |
| Source note | uspto-grants-2010_10 |