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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7406Generated: October 25, 2026

Hexane → 1-Benzyl-4-(1-phenethyl-1H-imidazol-2-YL)piperidin-4-OL

https://huagongshe.com/reaction/7406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant1-Benzyl-4-piperidoneHCID 19220—
Reactant1-(1-Phenylethyl)-1h-imidazoleHCID 9815351—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-4-(1-phenethyl-1H-imidazol-2-YL)piperidin-4-OLHCID 1132590475%

Reaction Conditions

Temperature-70 °C

Reaction Steps

A mixture of DIPA (1.4 mol) in THF (3000 ml) was stirred at −70° C. under N2 flow. Butyllithium 2.5 M/hexane (1.3 mol) was added portionwise at a temperature below −40° C. The mixture was stirred at −70° C. for 15 min. 1-phenylethyl-1H-imidazole (1 mol) dissolved in THF was added dropwise at a temperature below −55° C. The mixture was stirred at −70° C. for 1 hour. 1-(phenylmethyl)-4-piperidinone (1.2 mol) dissolved in THF was added dropwise at a temperature below −55° C. The mixture was stirred at −70° C. for 1 hour, then brought to room temperature, stirred at room temperature overnight and decomposed with H2O. The organic solvent was evaporated. The aqueous concentrate was extracted with CH2Cl2. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated. The residue was crystallized from DIPE (1100 ml). The precipitate was filtered off, washed with DIPE and dried, yielding 271 g of 4-[1-(2-phenylethyl)-1H-imidazol-2-yl]-1-(phenylmethyl)-4-piperidinol (75%) (interm. 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087595B2
Source datasetuspto-grants-2006_08
ORD IDord-b62c82ce4a9f497c902d1d7f12e1a2c2
Source noteuspto-grants-2006_08