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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377962Generated: October 31, 2026

Toluene → 1,2,2,6,6-Pentamethyl-4-(oxiran-2-ylmethoxy)piperidine

https://huagongshe.com/reaction/1377962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantEpichlorohydrinHCID 7835—
ReactantSodium HydroxideHCID 14798—
Reactant4-Piperidinol, 1,2,2,6,6-pentamethyl-HCID 75472—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
Product1,2,2,6,6-Pentamethyl-4-(oxiran-2-ylmethoxy)piperidineHCID 14274505—

Reaction Steps

300 g of sodium hydroxide (7.5 mol) are dissolved in 300 ml of water under an argon atmosphere in a 2.5 l sulfonation flask with a mechanical stirrer, condenser and 500 ml dropping funnel. 750 ml of toluene, 48.4 g (0.15 mol) of tetrabutylammonium bromide and 257 g (1.5 mol) of 4-hydroxy-l,2,2,6,6-pentamethylpiperidine are added. 347 g of epichlorohydrin (3.75 mol) are added dropwise at 60° C. in the course of 1.5 hours and the temperature is then kept at 60° C. for a further 4 hours, while stirring. The reaction solution is poured onto 3 1 of ice-water and the organic phase is separated off, dried with sodium sulfate and evaporated. The residue is distilled over a Vigreux column under 0.05 mmHg and the fraction of boiling point 71-72° C. is collected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665885
Source datasetuspto-grants-1997_09
ORD IDord-a22084280e25466391c76281c6601b8b
Source noteuspto-grants-1997_09