HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → [4-(3-Methoxyphenyl)-1-piperidinyl]acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | 4-(3-Methoxyphenyl)piperidine | HCID 10702890 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | [4-(3-Methoxyphenyl)-1-piperidinyl]acetonitrile | HCID 19597357 | 97% |
Reaction Steps
A mixture of bromoacetonitrile (0.70 mL, 10 mmol), 4-(3-methoxyphenyl)piperidine (1.74 g, 9.1 mmol) and K2CO3 (1.3 g) in MeCN was stirred at room temperature for 3 days. The reaction mixture was partitioned between CH2Cl2 and H2O, and the organic extract was dried (Na2SO4). The solvent was then removed in vacuo to afford [4-(3-methoxyphenyl)-1-piperidinyl]acetonitrile as an amber oil (2.03 g, 97%): MS (DCl) m/z 231 (MH+). Anal. Calcd. for C14H18N2O.0.5 H2O: C, 70.27; H, 8.00; N, 11.71. Found: C, 70.12; H, 7.67; N, 11.87.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06001836 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-b10a7b1104084050927bdf1883e6972d |
| Source note | uspto-grants-1999_12 |