HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 1-Methyl-3-cyclooctylmethylaminocarbonylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Cyclooctylmethylamine | HCID 78473 | — |
| Reactant | 1-Methylpiperidine-3-carboxylic acid hydrochloride | HCID 12514711 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-Methyl-3-cyclooctylmethylaminocarbonylpiperidine | HCID 20081674 | 62% |
Reaction Steps
To 80 ml of chloroform were added 3.59 g of 1-methylnipecotic acid hydrochloride and 6.26 ml of triethylamine. Thereto was added 3.0 g of isobutyl chloroformate under ice cooling and stirring. The mixture was stirred for 30 minutes. Thereto was added 3.1 g of cyclooctylmethylamine, and the mixture was subjected to a reaction for 2 hours at room temperature. The reaction mixture was washed with an aqueous sodium hydrogen carbonate solution and with water, and dried with anhydrous sodium sulfate. The solvent was removed by evaporation. The residue was purified by a Silica gel column chromatography (dichloromethane:methanol=10:1) to obtain 3.3 g of 1-methyl-3-cyclooctylmethylaminocarbonylpiperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05227381 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-fed3f7daeda94323b55fe02cec329d8c |
| Source note | uspto-grants-1993_07 |