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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858628Generated: November 1, 2026

Hydrochloric Acid → 1-Benzyl-4-[4-(2-hydroxy-ethyl)-phenyl]-piperidin-4-ol

https://huagongshe.com/reaction/1858628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
Reactant(RS)-1-benzyl-4-[4-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-phenyl]-piperidin-4-olHCID 22127334—
SolventMethanolHCID 887—
Product1-Benzyl-4-[4-(2-hydroxy-ethyl)-phenyl]-piperidin-4-olHCID 1490343884.1%

Reaction Steps

A solution of 78 g (197 mmol) of (RS)-1-benzyl-4-[4-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-phenyl]-piperidin-4-ol in 400 ml of methanol was treated with 470 ml of 2N hydrochloric acid and stirred at room temperature for 5 hours. For the working-up, the reaction solution was poured into 1500 ml of saturated sodium hydrogen carbonate solution and subsequently extracted three times with 1000 ml of ethyl acetate each time. The combined organic phases were dried over sodium sulphate and evaporated under reduced pressure. For purification of the crude substance, a flash chromatography on silica gel using a 95:5 mixture of methylene chloride and methanol as the eluent was carried out. There were obtained 51.6 g (84% of theory) of 1-benzyl-4-[4-(2-hydroxy-ethyl)-phenyl]-piperidin-4-ol as a yellowish solid; MS: 312 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150526
Source datasetuspto-grants-2000_11
ORD IDord-64b277fa0e304e648e023f289ac4c43c
Source noteuspto-grants-2000_11