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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863843Generated: October 31, 2026

Hydrogen Peroxide → 3-(2-Phenylethoxy)propan-1-ol

https://huagongshe.com/reaction/863843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
Reactant(2-Allyloxyethyl)benzeneHCID 84328—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Phenylethoxy)propan-1-olHCID 19082259—

Reaction Steps

To a cooled (0° C.) solution of 2-allyloxyethylbenzene (5. g; 30.8 mmol) dissolved in THF (75 ml) is slowly added a 0.5M THF solution of 9-BBN [9-borabicyclo[3.3.1]nonane] (68 ml; 34 mmol) and the reaction mixture warmed to room temperature and stirred for 4 hours. The reaction mixture is then cooled to 0° C. and 5 ml H2O is added followed by slow addition of 6N NaOH (30 ml; 7.2 g/30 ml). After stirring for 5 minutes, 30% H2O2 (20 ml)is added over 15 min. The reaction mixture warms significantly but is kept from refluxing. After addition is complete, it is stirred for 15 minutes allowing the mixture to come to room temperature. It is then diluted with Et2O, washed with H2O 2×, Na2S2O3 2×, NaHCO3 and brine, dried (MgSO4) and concentrated to dryness. The residue is purified by column chromatography using Et2O to obtain 3-(2-phenylethoxy)-1-propanol which is used directly in Step C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05561143
Source datasetuspto-grants-1996_10
ORD IDord-b9ce7379133940ce82098de21bbf5f0b
Source noteuspto-grants-1996_10