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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633412Generated: October 26, 2026

Hydrochloric Acid → 4-(4-Nitro-2-(trifluoromethyl)phenoxy)piperidine

https://huagongshe.com/reaction/633412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTert-butyl 4-(4-nitro-2-(trifluoromethyl)phenoxy)piperidine-1-carboxylateHCID 22181018—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product4-(4-Nitro-2-(trifluoromethyl)phenoxy)piperidineHCID 2073538190%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of tert-butyl 4-(4-nitro-2-(trifluoromethyl)phenoxy)piperidine-1-carboxylate (1.4 g, 1.0 eq, 3.6 mmol) in CH2Cl2 (25 mL) was cooled to 0° C. while stifling. 4N HCl in dioxane (15 mL) was added to the above solution and stirred at 0° C. for 30 minutes and brought to room temperature for 2 hours. The volatiles were removed under vacuum to leave a crude solid. The crude mixture was dissolved in EtOAc (100 mL) and partitioned with 1N aqueous NaOH solution (50 mL). Organic layers were separated and the aqueous layer was washed with EtOAc (50 mL). The combined organic layers were dried over Na2SO4 and concentrated under vacuum to give the desired product in 90% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321763B2
Source datasetuspto-grants-2016_04
ORD IDord-36f697c62a644954a1072d4dac02887d
Source noteuspto-grants-2016_04