HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 1-[4-(16-Bromohexadecylamino)benzoyl]piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 4-(16-Bromohexadecylamino)benzoyl chloride hydrochloride | HCID 13025408 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-[4-(16-Bromohexadecylamino)benzoyl]piperidine | HCID 13025411 | — |
Reaction Steps
To a chilled solution of 35 ml. of piperidine, 2.5 ml. of triethylamine and 0.6 g. of dimethylaminopyridine in 100 ml. of diethyl ether is added (1/2 hour) a solution of 8.3 g. of 4-(16-bromohexadecylamino)benzoyl chloride hydrochloride in 50 ml. of ether. The solution is warmed to room temperature and maintained there for two hours. The solution is heated to reflux for an additional 2 hours at which time the reaction is complete. The solution is cooled, extracted twice with 100 ml. portions of water and dried over magnesium sulfate. The solvent is removed in vacuo and the solid is recrystallized in 50 ml. of diethyl ether to yield the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04245097 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-1ae56a8d1f3b459ebcafbe33b86393dc |
| Source note | uspto-grants-1981_01 |