HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-Ethyl-2-(4-chlorobenzyl)perhydroazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-[(4-Chlorophenyl)methyl]azepane | HCID 3933809 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 1-Ethyl-2-(4-chlorobenzyl)perhydroazepine | HCID 23342803 | — |
Reaction Steps
Boil together (under agitation) 4 g of 2-(4-chlorobenzyl)perhydroazepine, 2.5 g of anhydrous potassium carbonate and 2.9 g of ethyl bromide under reflux for 26 hours in 30 ml of ethylmethylketone. Cool the thus-produced reaction mixture to ambient temperature. Mix the cooled reaction mixture with water and then extract it with diethyl ether. Dry the resulting organic phase over sodium sulfate, remove the ether and distil the residue to obtain 5.12 g (70% of theory) of the title compound with a BP of 112° at 0.005 mm of Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04221788 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-61b6237faed14f6ea997de5e8a8ecfe3 |
| Source note | uspto-grants-1980_09 |