HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 12612263, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 3-(2-Chloroethyl)-3-azabicyclo[3.2.2]nonane | HCID 16146 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | 4-Diisopropylamino-2-phenyl-butyronitrile | HCID 12612210 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12612263 | HCID 12612263 | — |
Reaction Steps
A solution of 16 parts of α-[2-(diisopropylamino)ethyl]-α-phenylacetonitrile and 5 parts of sodium amide in 200 parts by volume of toluene is heated to about 100° C. over a period of 15 minutes and then 20 parts of 3-(2-chloroethyl)-3-azabicyclo[3.2.2]nonane in 100 parts by volume of toluene is added slowly over a period of 20 minutes. This mixture is heated at 105°-110° C. for an hour and then cooled to room temperature when 200 parts by volume of water is added. The organic layer is separated, dried over calcium sulfate, concentrated, and then distilled to afford 2-[2-(diisopropylamino)ethyl]-2-phenyl-4-(3-azabicyclo[3.2.2]non-3-yl)butyronitrile, as an oil. This compound is represented by the following structural formula ##STR16##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04134890 |
| Source dataset | uspto-grants-1979_01 |
| ORD ID | ord-1e84d29fbd134120be10a46306061ab2 |
| Source note | uspto-grants-1979_01 |