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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35597Generated: October 25, 2026

4-Bromobutyronitrile → 4-(2-Chloro-3-piperidinomethylphenoxy)butyronitrile

https://huagongshe.com/reaction/35597

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobutyronitrileHCID 21412—
ReactantN-(2-chloro-3-hydroxybenzyl)piperidineHCID 21294597—
Product4-(2-Chloro-3-piperidinomethylphenoxy)butyronitrileHCID 21294553—

Reaction Steps

In a similar manner to that described in Example 17 2-chloro-3-hydroxybenzaldehyde (9 g) in absolute ethanol (60 ml) was treated with piperidine (11.7 ml) and sodium borohydride (2.2 g) to yield N-(2-chloro-3-hydroxybenzyl)piperidine. The piperidine thus prepared was reacted with 4-bromobutyronitrile to give 4-(2-chloro-3-piperidinomethylphenoxy)butyronitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767769
Source datasetuspto-grants-1988_08
ORD IDord-83f7587f3fc4437aabe7bd529e5d8791
Source noteuspto-grants-1988_08