HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → trans-1-{3-[4-(Methoxycarbonyl)phenoxy]propyl}-3,5-dimethylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3S,5S)-3,5-dimethylpiperidine | HCID 7058087 | — |
| Reactant | Methyl 4-(3-chloropropoxy)benzoate | HCID 12389265 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | trans-1-{3-[4-(Methoxycarbonyl)phenoxy]propyl}-3,5-dimethylpiperidine | HCID 68912339 | — |
Reaction Steps
A mixture of methyl 4-(3-chloropropoxy)benzoate (4.57 g), potassium carbonate (8.29 g), cis and trans-3,5-dimethylpiperidine (5.31 mL) and a catalytic amount of potassium iodide in N,N-dimethylformamide (100 mL) is stirred overnight at 100° C. The suspension is filtrated and the precipitate washed with ethanol. The filtrate is concentrated under reduced pressure and purified by chromatography over silica gel with a gradient of dichloromethane/methanol from 98/2 to 90/10. Fraction containing the expected products are pooled and concentrated under reduced pressure yielding 5.33 g of cis and trans-1-{3-[4-(methoxycarbonyl)phenoxy]propyl}-3,5-dimethylpiperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08076329B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-d28c0c4ebf7844b790bdafa7b1182557 |
| Source note | uspto-grants-2011_12 |