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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435956Generated: November 2, 2026

Potassium bisulfate → 5-(3-Benzyloxy-propyl)-piperidine-2,4-dione

https://huagongshe.com/reaction/1435956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bisulfateHCID 516920—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantBenzyl 3-Bromopropyl EtherHCID 2776064—
Reactanttert-Butyl 2,4-dioxopiperidine-1-carboxylateHCID 23730999—
SolventTetrahydrofuranHCID 8028—
Product5-(3-Benzyloxy-propyl)-piperidine-2,4-dioneHCID 6907531382%

Reaction Steps

To a solution of tert-butyl 2,4-dioxopiperidine-1-carboxylate (3.84 g, 18 mmol) in anhydrous THF (100 mL), cooled at −20° C. under nitrogen atmosphere, 1M LiHMDS in THF (54 mL) was added dropwise. After 20 min under stirring, (3-bromo-propoxymethyl)-benzene (54 mmol) was added and the solution was stirred at −20° C. for 2 hours. The reaction mixture was poured into 5% aq. KHSO4 and extracted with DCM two times. The collected organic layers were concentrated to 500 mL and 50 mL of TFA were added. The resulting solution was stirred at room temperature for 1 hour. After evaporation, the residue was purified by column chromatography (hexane/EtOAc 1:2) affording 3.85 g of the title compound (14.7 mmol, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618982B2
Source datasetuspto-grants-2009_11
ORD IDord-7f306e4980874d0fb9b4004766e54f37
Source noteuspto-grants-2009_11