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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209628Generated: October 31, 2026

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

https://huagongshe.com/reaction/2209628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
Reactant(2-Allyloxyethyl)benzeneHCID 84328—
SolventWaterHCID 962—
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 numberUS05455260
Source datasetuspto-grants-1995_10
ORD IDord-4082fa8a85f04045b3a89493fd8e88d9
Source noteuspto-grants-1995_10