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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024365Generated: October 29, 2026

Hydrogen Peroxide → 8-Benzyl-2,3,8-triaza-spiro[4.5]dec-2-ene

https://huagongshe.com/reaction/1024365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantMethanolHCID 887—
Reactant(1-Benzylpiperidine-4,4-diyl)dimethanamineHCID 12326861—
ReactantSodium HypochloriteHCID 23665760—
SolventWaterHCID 962—
Product8-Benzyl-2,3,8-triaza-spiro[4.5]dec-2-eneHCID 5659406190.3%

Reaction Steps

2.48 g of C-(4-Aminomethyl-1-benzyl-piperidin-4-yl)-methylamine was suspended in 40 mL H2O and 10 mL MeOH and cooled with an ice bath. Simultaneously, 6.7 mL 30% H2O2 (6 equiv.) and 15.2 mL 10% NaClO (2.4 equiv.) were added dropwise. The mixture was stirred at room temperature for 1 hour. The mixture was extracted 2 times with DCM, the combined organic layers were dried over Na2SO4, filtrated and concentrated to yield 2.20 g of a yellow oil which was used without further purification in the subsequent step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722887B2
Source datasetuspto-grants-2014_05
ORD IDord-3d38630b0d6044e0993a671856066298
Source noteuspto-grants-2014_05