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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336227Generated: October 27, 2026

Lithium Hydroxide → 4-(Piperidin-1-yl)benzoic acid

https://huagongshe.com/reaction/336227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantPiperidineHCID 8082—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 4-fluorobenzoateHCID 67878—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product4-(Piperidin-1-yl)benzoic acidHCID 764599—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of methyl 4-fluorobenzoate (Lancaster 14154; 500 mg; 3.24 mmol; 1 eq.) and piperidine (Fluka 80640; 828.62 mg; 9.73 mmol; 3 eq.) in DMF (2 mL) was stirred at 50° C. for 16 hours. The reaction mixture was then passed through a short pad of silica and the obtained solution evaporated in vacuo to give a colourless oil. The oil was taken up in THF (15 mL) and lithium hydroxide (388.41 mg; 16.22 mmol; 5 eq.) was added followed by water (15 mL). The reaction mixture was stirred at room temperature for 6 hours then at 60° C. for 16 hours. NaOH (155.5 mg, 6.48 mmol, 2 eq) was then added and the reaction mixture was refluxed for 24 hours. After cooling, the solution was diluted with water and washed with Et2O. The aqueous layer was then acidified to pH 5-6 with acetic acid and the formed precipitate was collected by filtration, washed with water and dried under high vacuum to afford the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889668B2
Source datasetuspto-grants-2014_11
ORD IDord-2230f89093db4e649b0bbaea6606ee11
Source noteuspto-grants-2014_11