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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967766Generated: October 31, 2026

Water → 1-[2-(4-Cyanophenyl)ethyl]-4-(4-hydroxymethylphenoxymethyl)piperidin-4-ol

https://huagongshe.com/reaction/967766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant1-[2-(4-Cyanophenyl)ethyl]-4-(4-formylphenoxymethyl)piperidin-4-olHCID 22291295—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product1-[2-(4-Cyanophenyl)ethyl]-4-(4-hydroxymethylphenoxymethyl)piperidin-4-olHCID 996915879.6%

Reaction Steps

The compound (0.20 g) obtained in Step 1 was dissolved in a mixture of ethanol (3 mL) and tetrahydrofuran (2.75 mL) and to this solution was added sodium borohydride (0.016 g) under cooling with ice-water and the mixture was stirred at the same temperature for two hours under nitrogen atmosphere. After adding water (15 mL) and stirring, to the mixture was added salt until it was saturated, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (Chromatorex NH™) (eluent; ethyl acetate:methanol=99:1 to 9:1) to obtain the titled compound (0.16 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06956046B2
Source datasetuspto-grants-2005_10
ORD IDord-4f2eb161733649c29e5af72a0f020f30
Source noteuspto-grants-2005_10