HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(2-Chlorophenyl)-4-(diisopropylamino)butanenitrile → alpha-(o-Chlorophenyl)-alpha-[2-(diisopropylamino)ethyl]-alpha-(2-piperidinoethyl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(2-Chlorophenyl)-4-(diisopropylamino)butanenitrile | HCID 12612211 | — |
| Reactant | alpha-(o-Fluorophenyl)-alpha-[2-(diisopropylamino)ethyl]acetonitrile | HCID 12612212 | — |
| Product | alpha-(o-Chlorophenyl)-alpha-[2-(diisopropylamino)ethyl]-alpha-(2-piperidinoethyl)acetonitrile | HCID 12612239 | — |
Reaction Steps
When an equivalent quantity of α-(o-chlorophenyl)-α-[2-(diisopropylamino)ethyl]acetonitrile prepared according to the first paragraph of Example 19, is substituted for α-(o-fluorophenyl)-α-[2-(diisopropylamino)ethyl]acetonitrile called for in Example 20 and the procedure detailed in the second paragraph of that example is substantially repeated, there is obtained α-(o-chlorophenyl)-α-[2-(diisopropylamino)ethyl]-α-(2-piperidinoethyl)acetonitrile, as an oil boiling at about 190°-195° C. at 0.3 mm. pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04107205 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-1471ade7658d4fdd86891d886eb601e2 |
| Source note | uspto-grants-1978_08 |