HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N,N',N'-Tetramethylethylenediamine → HCID 22759855, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | 1-Bromohexane | HCID 8101 | — |
| Reactant | HCID 20339673 | HCID 20339673 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 22759855 | HCID 22759855 | — |
Reaction Steps
Following the procedure which is described in Example 4, 2.91 parts of 2-(2,2-diphenylethyl)-1-azabicyclo[2.2.2]octane in 40 parts by volume of cyclohexane, 5.1 parts by volume of a 2.17 M solution of butyl lithium in hexane are reacted with 1.5 parts of TMEDA and 1.81 parts of n-hexyl bromide to provide 2-(2,2-diphenyloctyl)-1-azabicyclo[2.2.2]octane. This compound is then treated with 0.730 parts of maleic acid to give 2-(2,2-diphenyloctyl)-1-azabicyclo[2.2.2]octane maleate, melting at about 180°-181° C. This compound is represented by the following structural formula ##STR10##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04125531 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-a35a5fae473a4ce18fdd81e67eabc9c3 |
| Source note | uspto-grants-1978_11 |