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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696821Generated: October 28, 2026

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

https://huagongshe.com/reaction/1696821

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 stiffing 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 numberUS08163775B2
Source datasetuspto-grants-2012_04
ORD IDord-a0d7a6b4dda649ce8dc6a5920f0c4a96
Source noteuspto-grants-2012_04