HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → HCID 13472123, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 13472122 | HCID 13472122 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | HCID 13472123 | HCID 13472123 | — |
Reaction Steps
1-(6-bromohexanoyl)-1,2,3,4-tetrahydroquinoline, (4.9 g), prepared in a manner similar to that set forth in Preparation 1, was refluxed, using a dry ice condenser, in a saturated solution of dimethylamine in ethylene glycol (46 ml). After 45 minutes the solution was cooled and added to dilute aqueous potassium hydroxide. The resultant solution was extracted with ether, and the extract was washed, dried and evaporated to yield as an oil 1-(6-dimethylaminohexanoyl)-1,2,3,4-tetrahydroquinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04512990 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-24f7a7f18e05437d9e8f633c6f63a8b9 |
| Source note | uspto-grants-1985_04 |