HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylpiperidine → HCID 19907488, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylpiperidine | HCID 12291 | — |
| Reactant | HCID 15284075 | HCID 15284075 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19907488 | HCID 19907488 | 171.1% |
Reaction Steps
First, 0.35 g of 1,4-bis(4-bromobutyl)benzene and 0.5 g of N-methylpiperidine were dissolved in 5 ml of absolute ethanol, the solution was refluxed for 9 hours, and evaporated under a reduced pressure. To the residue were added acetone and a small amount of ethanol, and the mixture was stirred at a room temperature for 30 minutes. The resulting crystal was filtered, washed with acetone and dried under a reduced pressure to obtain 0.47 g of the title compound as a colorless crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05093370 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-cca3eec2403c4236951c1c36de456516 |
| Source note | uspto-grants-1992_03 |