HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Propylpiperidine → 4-(2-Propyl-piperidin-1-yl)-butyronitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Propylpiperidine | HCID 9985 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromobutyronitrile | HCID 21412 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 4-(2-Propyl-piperidin-1-yl)-butyronitrile | HCID 18626322 | 83% |
Reaction Steps
A mixture of 2-propylpiperidine (550 mg, 4.3 mmol), 4-bromobutyronitrile (430 mg, 3.0 mmol) and potassium carbonate (550 mg, 4.0 mmol) in acetonitrile (5 mL) was stirred at rt for 12 h., followed by addition of a saturated brine (25 mL). The reaction mixture was extracted with ethyl acetate (3×25 mL) and the combined organic phases were dried (MgSO4) and evaporated to dryness to produce crude 8. The crude product was subjected to CC [eluent: CH2Cl2: MeOH (99: 1)] to give pure 8 (0.48 g, 83%); LC-MS [M+H]+ 194 (cald. 194.2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07485651B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-bc522ddd6f44485c9a1863fa5aae7e5b |
| Source note | uspto-grants-2009_02 |