Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708624Generated: November 3, 2026

Hydrogen Peroxide → HCID 23372103, compound

https://huagongshe.com/reaction/1708624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
Reactant4-Allyloxy-1-octyloxy-2,2,6,6-tetramethylpiperidineHCID 23372106—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23372103HCID 2337210389%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 14.9 grams (45.9 mmol) of 4-allyloxy-1-octyloxy-2,2,6,6-tetramethylpiperidine (prepared in Example 10A) in 20 ml of anhydrous tetrahydrofuran is added over a 10-minute period to a solution of 5.6 grams (45.9 mmol) of 9-borabicyclo [3.3.1]nonane in 20 ml of tetrahydrofuran under a nitrogen atmosphere. The reaction mixture is cooled to 20° C. and a solution of 1.84 gram (45.9 mmol) of sodium hydroxide in water is added over a 10-minute period. A solution of 15.3 ml of 30% aqueous hydrogen peroxide is then added over 30 minutes while the reaction mixture is cooled in an ice-water bath. The reaction mixture is diluted with ether (50 ml) and the organic layer is separated and dried over potassium carbonate. Solvent is evaporated and the residue is purified by flash chromatography (silica gel; 2:1 heptane: ethyl acetate) to afford 14.0 grams (89 % yield) of the title compound is a colorless syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05359069
Source datasetuspto-grants-1994_10
ORD IDord-deed29829bd3431e933c4ac17d3175a8
Source noteuspto-grants-1994_10