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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172761Generated: November 3, 2026

Hydrochloric Acid → (4-Fluorophenyl)(3-hydroxypiperidin-1-yl)methanone

https://huagongshe.com/reaction/1172761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant4-Fluorobenzoic AcidHCID 9973—
Reactant3-HydroxypiperidineHCID 23293—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDichloromethaneHCID 6344—
Product(4-Fluorophenyl)(3-hydroxypiperidin-1-yl)methanoneHCID 4578648053%

Reaction Steps

A mixture of 3-hydroxypiperidine (0.6 g, 5.93 mmol), 4-fluorobenzoic acid (0.83 g, 5.93 mmol), HOBT (0.8 g, 5.93 mmol), EDCI.HCl (1.7 g, 8.9 mmol) and dry triethylamine (1.66 mL, 11.86 mmol) in dry dichloromethane (30 mL) was kept under stirring overnight at ambient temperature, under nitrogen atmosphere. HCl 1N (30 mL) was then added and the phases separated. The organic layer was washed with HCl 1N (30 mL), with NaOH 1N (30 mL×2 times), then with water (30 mL). Evaporation of the organic solvent afforded (4-fluoro-phenyl)-(3-hydroxy-piperidin-1-yl)-methanone as a white oil (0.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834035B2
Source datasetuspto-grants-2010_11
ORD IDord-d354b783a6534016b94dfe4f80820ffd
Source noteuspto-grants-2010_11