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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419612Generated: October 31, 2026

2-(2-Chlorophenyl)-4-(diisopropylamino)butanenitrile → alpha-(o-Chlorophenyl)-alpha-[2-(diisopropylamino)ethyl]-alpha-(2-piperidinoethyl)acetonitrile

https://huagongshe.com/reaction/2419612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Chlorophenyl)-4-(diisopropylamino)butanenitrileHCID 12612211—
Reactantalpha-(o-Fluorophenyl)-alpha-[2-(diisopropylamino)ethyl]acetonitrileHCID 12612212—
Productalpha-(o-Chlorophenyl)-alpha-[2-(diisopropylamino)ethyl]-alpha-(2-piperidinoethyl)acetonitrileHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04107205
Source datasetuspto-grants-1978_08
ORD IDord-1471ade7658d4fdd86891d886eb601e2
Source noteuspto-grants-1978_08