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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371140Generated: November 1, 2026

Ethyl 1-benzylpiperidine-3-carboxylate → (1-Benzylpiperidin-3-yl)methanol

https://huagongshe.com/reaction/2371140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1-benzylpiperidine-3-carboxylateHCID 2736370—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(1-Benzylpiperidin-3-yl)methanolHCID 1039804499%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of ethyl 1-benzylpiperidine-3-carboxylate (1.0 g) in tetrahydrofuran (10 mL) at 5° C. under argon was added a 1M solution of lithium aluminium hydride (4.04 mL) dropwise. The mixture was stirred for 1 hour at 5° C. and then quenched by the dropwise addition of ethyl acetate (5 mL). The mixture was warmed to room temperature and dichloromethane (150 mL) was added followed by saturated aqueous sodium potassium tartrate (50 mL). The mixture was stirred vigorously overnight. The layers were separated and the organic layer was dried over magnesium sulfate and evaporated to give the title compound as a colourless oil (0.82 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710224B2
Source datasetuspto-grants-2014_04
ORD IDord-b825fd0aa3d8434ea4ac158e4cc9434c
Source noteuspto-grants-2014_04