HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 3,5-Dimethyl-1-(3-Methyl-4-Nitrobenzyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,5-Dimethylpiperidine | HCID 118259 | — |
| Reactant | 3-Methyl-4-nitrobenzyl bromide | HCID 4445978 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3,5-Dimethyl-1-(3-Methyl-4-Nitrobenzyl)piperidine | HCID 53358552 | 61% |
Reaction Steps
3-Methyl-4-nitrobenzyl bromide (1.00 g), 3,5-dimethylpiperidine (0.60 ml) and potassium carbonate (0.90 g) were dissolved in acetone (20 ml), followed by heating under reflux for 6 hours. The reaction solution was concentrated under reduced pressure, dissolved in chloroform (10 ml), poured into water (100 ml) and extracted with chloroform (50 ml). The organic layer was washed with saturated brine (100 ml), dried over anhydrous sodium sulfate and, after filtration, concentrated under reduced pressure. The residue was purified by silica gel flash column chromatography (developing solvent: n-hexane/ethyl acetate=10:1) to obtain the subject compound (NCR-7) (0.70 g, yield 61%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09206125B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-2b9d2d25a2154c028c5f4e8e61c44dbe |
| Source note | uspto-grants-2015_12 |