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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633413Generated: October 26, 2026

Sodium Bicarbonate → 4-(4-Nitro-2-(trifluoromethyl)phenoxy)-1-(oxetan-3-yl)piperidine

https://huagongshe.com/reaction/633413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-OxetanoneHCID 15024254—
Reactant4-(4-Nitro-2-(trifluoromethyl)phenoxy)piperidineHCID 20735381—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
Product4-(4-Nitro-2-(trifluoromethyl)phenoxy)-1-(oxetan-3-yl)piperidineHCID 8670450777%

Reaction Steps

A solution of 4-(4-nitro-2-(trifluoromethyl)phenoxy)piperidine (1.0 g, 1.0 eq, 3.5 mmol) and oxetan-3-one (0.35 g, 1.4 eq, 4.8 mmol) in 1,2-dichloroethane (50 mL) was stirred at room temperature for 30 minutes. Sodium triacetoxyborohydride (1.3 g, 1.8 eq, 6.2 mmol) was added in portions to the above solution and the heterogeneous mixture was stirred at room temperature overnight. The reaction mixture was diluted with CH2Cl2 (50 mL) and pardoned with aqueous saturated NaHCO3 solution (100 mL). The layers were separated and the organic layer was washed with brine solution (2×50 mL). The combined organic layers were dried over Na2SO4. Removal of the solvents and purification of the crude mixture by column chromatography on silica gel (ISCO System) using 20% MeOH in CH2Cl2/CH2Cl2 (gradient system from 0:1 to 1:9) as eluent gave the product in 77% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321763B2
Source datasetuspto-grants-2016_04
ORD IDord-2633f3fca6f54aec92bb7b414a9677b9
Source noteuspto-grants-2016_04