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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419934Generated: October 31, 2026

Water → 1-(2-Hydroxy-ethyl)-4-(4-methyl-benzyl)-piperidin-4-ol

https://huagongshe.com/reaction/1419934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-BromoethanolHCID 10898—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Methylbenzyl)-piperidin-4-olHCID 10536242—
SolventMethyl Ethyl KetoneHCID 6569—
Product1-(2-Hydroxy-ethyl)-4-(4-methyl-benzyl)-piperidin-4-olHCID 5424264473%

Reaction Steps

A mixture containing 4-(4-methyl-benzyl)-piperidin-4-ol (5.1 g, 25 mmol), 2-bromoethanol (1.8 ml, 25 mmol) and K2CO3 (5.2 g, 37.5 mmol) in 2-butanone (120 ml) was refluxed for 22 hours. H2O (30 ml) was added and the aqueous phase was extracted with ethylacetate. Combined organic phases were dried over Na2SO4, and concentrated. The residue was chromatographed over silica gel (CH2Cl2 --MeOH, 9:1 +NH4OH (1%)) to provide 1-(2-hydroxy-ethyl)-4-(4-methyl-benzyl)-piperidin-4-ol (4.3 g, 73%) as a yellow oil, MS: m/e=235.3 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05889026
Source datasetuspto-grants-1999_03
ORD IDord-a8e9398e02fe4181bd2c8533d7b06be0
Source noteuspto-grants-1999_03