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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209103Generated: October 30, 2026

Diisopropylethylamine → 4-(4-Bromophenyl)-1-(oxetan-3-yl)piperidine

https://huagongshe.com/reaction/2209103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(4-Bromophenyl)piperidineHCID 2757159—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-OxetanoneHCID 15024254—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Bromophenyl)-1-(oxetan-3-yl)piperidineHCID 11784373157%

Reaction Steps

In a round-bottomed, single-necked, 100-mL flask were placed 4-(4-bromophenyl)piperidine (500.0 mg, 2.08 mmol), N,N-diisopropylethylamine (0.36 mL, 2.08 mmol), 3-oxetanone (0.27 mL, 4.16 mmol), and sodium triacetoxyborohydride (1544.5 mg, 7.3 mmol) in THF (15 mL). The mixture was stirred at room temperature for 16 h. Then, it was quenched with water and the organic layers extracted with EtOAc (3×5 mL). The combined organic layers were washed with water (2×5 mL) and brine (1×5 mL), dried (Na2SO4), concentrated, and purified by flash chromatography (100% Hexane to 100% EtOAc) to give 350.0 mg (57%) of 4-(4-bromophenyl)-1-(oxetan-3-yl)piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376441B2
Source datasetuspto-grants-2016_06
ORD IDord-73ebde737e244788adb7866841dbbbeb
Source noteuspto-grants-2016_06