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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294095Generated: October 30, 2026

Hydrogen Peroxide → Tert-butyl 4-(2-hydroxyethyl)benzoate

https://huagongshe.com/reaction/2294095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
Reactantt-Butyl 4-vinylbenzoateHCID 9990491—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(2-hydroxyethyl)benzoateHCID 10331132—

Reaction Steps

A solution of 9-borabicyclo[3.3.1]nonane (9-BBN, 5.65 g, 46.3 mmol) in anhydrous tetrahydrofuran was added to a solution of t-butyl 4-vinylbenzoate (8.47 g, 42.1 mmol) prepared in the Preparative Example 102 in anhydrous tetrahydrofuran in a nitrogen stream. The obtained mixture was stirred at room temperature for 3 hours. 15 ml of water and 17 ml of 3N NaOH were added to the reaction mixture successively, followed by the dropwise addition of 80% aqueous hydrogen peroxide at 50° C. or below. The obtained mixture was stirred as such for one hour and poured into water. The mixture thus obtained was extracted with ethyl acetate. The organic phase was washed with an aqueous solution of common salt, dehydrated and distilled to remove the solvent. The obtained residue was purified by silica gel column chromatography (developer: n-hexane/ethyl acetate=1:1) to give the objective compound. yield: 8.71 g

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688800
Source datasetuspto-grants-1997_11
ORD IDord-1e910c7c2ecf457b901f75f10e650e9c
Source noteuspto-grants-1997_11