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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511095Generated: November 1, 2026

Hydrochloric Acid → Hydrochloric Acid

https://huagongshe.com/reaction/511095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Fluoro-2-nitrobenzotrifluorideHCID 223094—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventDimethyl SulfoxideHCID 679—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHydrochloric AcidHCID 313—
Product4-(4-Nitro-3-trifluoromethyl-phenoxy)-piperidine hydrochlorideHCID 66671759—

Reaction Steps

A solution of 4-hydroxy-piperidine-1-carboxylic acid tert-butyl ester (2.2 g; 11.0 mmol), 5-fluoro-2-nitrobenzotrifluoride (2.5 g; 11.9 mmol) and potassium carbonate (3.0 g; 22.0 mmol) in dimethylsulfoxide (25 mL) is heated over night at 100° C. The mixture is then diluted with dichloromethane (200 mL) and is washed with water (25 mL), aq. sat. ammonium chloride (25 mL) and twice with water (25 mL). The organic layer is then filtered and the filtrate is evaporated under reduced pressure. The product is dissolved in a 1 to 1 mixture of dichloromethane and trifluoroacetic acid (16 mL) and the resulting solution is stirred at room temperature until complete conversion is observed (about 30 minutes). After concentration under reduced pressure, the residue obtained is co-evaporated with dichloromethane (3×30 mL). The crude product is diluted in diethylether (25 mL) and a molar solution of hydrochloric acid in diethylether (15 mL) is added under stirring. The solid obtained is finally filtered and is dried under high vacuum to yield the desired product as hydrochloride (1.86 g; 5.7 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096524B2
Source datasetuspto-grants-2015_08
ORD IDord-8af0b7530f514915b61cc883e7ddbcc0
Source noteuspto-grants-2015_08