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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422182Generated: November 1, 2026

1,4-Dihydroxy-2,2,6,6-tetramethylpiperidine → HCID 57120762, compound

https://huagongshe.com/reaction/1422182

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dihydroxy-2,2,6,6-tetramethylpiperidineHCID 5395—
ReactantAllyl bromideHCID 7841—
ReactantSodium HydroxideHCID 14798—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
ProductHCID 57120762HCID 57120762—

Reaction Conditions

Temperature70 °C

Reaction Steps

A vigorously stirred two phase solution of 30.0 g (0.17 mol) 1-oxyl-2,2,6,6-tetramethyl-4-hydroxypiperidine, 29.0 g (0.24 mol) of allyl bromide, 2.6 g (8 mmol) of tetrabutylammonium bromide, 100 mL of 50% aqueous sodium hydroxide and 30 mL of toluene is heated at 70° C. for 90 minutes. The mixture is partitioned between 100 mL of toluene, 100 mL of heptane and 200 mL of water. The organic phase is dried over anhydrous magnesium sulfate and concentrated to yield the title compound as a red oil after column chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080864
Source datasetuspto-grants-2000_06
ORD IDord-324564ea8355468abecd563dad69d6ab
Source noteuspto-grants-2000_06