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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35596Generated: October 24, 2026

Piperidine → N-(2-chloro-3-hydroxybenzyl)piperidine

https://huagongshe.com/en/reaction/35596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant2-Chloro-3-hydroxybenzaldehydeHCID 593376—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
ProductN-(2-chloro-3-hydroxybenzyl)piperidineHCID 21294597—

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-a40479b1925649b88b9ca5b70f57c52c
Source noteuspto-grants-1988_08