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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612841Generated: November 2, 2026

Sulfuric Acid → 4-(Phenyl-2-pyridylmethoxy)-1-[3-(2-nitrophenoxy)propyl]piperidine

https://huagongshe.com/reaction/1612841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantPhenyl(pyridin-2-yl)methanolHCID 315585—
Reactant4-Hydroxy-1-[3-(2-nitrophenoxy)propyl]piperidineHCID 19776793—
SolventTolueneHCID 1140—
Product4-(Phenyl-2-pyridylmethoxy)-1-[3-(2-nitrophenoxy)propyl]piperidineHCID 1977681929.3%

Reaction Conditions

Temperature120 °C

Reaction Steps

There was stirred at 120° C. for 4 hours a mixture of 6.74 g of phenyl-2-pyridylmethanol, 7.85 g of 4-hydroxy-1-[3-(2-nitrophenoxy)propyl]piperidine, 11.0 g of concentrated sulfuric acid and 15 ml of toluene. After cooling, the reaction solution was poured into ice water, made alkaline with an aqueous sodium hydroxide, and extracted with toluene. The extract was washed with water, and toluene was removed under reduced pressure. The residue was eluted with ethyl acetate-ethanol-dichloromethane (1:1:1) by silica gel column chromatography to give 3.67 g of oily 4-(phenyl-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-5c072b6699774af5b33fab6be2d33b39
Source noteuspto-grants-1993_03