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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272277Generated: November 1, 2026

Hexane → 1-Benzyl-4-(3,4-dimethoxyphenyl)piperidin-4-ol

https://huagongshe.com/reaction/1272277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantBenzene, 4-bromo-1,2-dimethoxy-HCID 76114—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-4-(3,4-dimethoxyphenyl)piperidin-4-olHCID 1353556571%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of n-butyllithium in hexane (1.56 M, 93.0 mL, 145 mmol) was added dropwise a solution of 4-bromo-1,2-dimethoxybenzene (34.4 g, 158 mmol) in THF (350 ml) under −70° C. and stirred for 30 minutes under argon atmosphere. A solution of 1-benzyl piperidin-4-one (25.0 g, 132 mmol) in THF (50 ml) was added dropwise to the reaction mixture under −60° C., and the mixture was allowed to warm to 0° C. and stirred under ice cooling for 30 minutes. The reaction mixture was diluted with water, concentrated under reduced pressure, and extracted with ethyl acetate. The organic extract was washed with water and saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified using silica gel column chromatography and the obtained crystals were washed with hexane to obtain 26.6 g (yield 71%) of the title compound. mp. 112–114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208495B2
Source datasetuspto-grants-2007_04
ORD IDord-a784dea104e5474d870d832e022c9a72
Source noteuspto-grants-2007_04