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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612842Generated: November 3, 2026

(4-Chlorophenyl)(pyridin-2-yl)methanol → 4-[(4-Chlorophenyl)-2-pyridylmethoxy]-1-[3-(2-nitrophenoxy)propyl]piperidine

https://huagongshe.com/reaction/1612842

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Chlorophenyl)(pyridin-2-yl)methanolHCID 97719—
Reactant4-Hydroxy-1-[3-(2-nitrophenoxy)propyl]piperidineHCID 19776793—
Product4-[(4-Chlorophenyl)-2-pyridylmethoxy]-1-[3-(2-nitrophenoxy)propyl]piperidineHCID 19776734—

Reaction Steps

The procedure of Example 32 (a) was repeated except for using (4-chlorophenyl)-2-pyridylmethanol and 4-hydroxy-1-[3-(2-nitrophenoxy)propyl]piperidine instead of phenyl-2-pyridylmethanol and 4-hydroxy-1-[3-(2-nitrophenoxy)propyl]piperidine to give oily 4-[(4-chlorophenyl)-2-pyridylmethoxy]-1-[3-(2-nitrophenoxy)propyl]piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05190959
Source datasetuspto-grants-1993_03
ORD IDord-e03fa41095934e95b9d151b2edf5870d
Source noteuspto-grants-1993_03