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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069038Generated: October 27, 2026

Hydrogen Peroxide → tert-Butyl 4-(2-hydroxyethyl)naphthalen-1-ylcarbamate

https://huagongshe.com/reaction/2069038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
Reactanttert-Butyl 4-vinylnaphthalen-1-ylcarbamateHCID 68313610—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-(2-hydroxyethyl)naphthalen-1-ylcarbamateHCID 6831387986.2%

Reaction Steps

To a solution of tert-butyl 4-vinylnaphthalen-1-ylcarbamate (31) (0.83 g, 3.08 mmol) in THF (10 mL) was added 9-BBN (0.5M in THF, 9.9 mL, 4.95 mmol) dropwise under nitrogen at 0° C. The mixture was warmed to RT and stirred for 16 hr. Water (1 mL), aqueous NaOH solution (3M, 10.0 mL, 30 mmol) and hydrogen peroxide (35% in water, 8.0 mL) were added. The reaction mixture was warmed to 50° C. and stirred for 2 hr and was then extracted with ethyl acetate. The ethyl acetate extract was washed with water and brine, dried (MgSO4) and evaporated in vacuo. The residue was purified by flash column chromatography (SiO2, 10-60% ethyl acetate in isohexane, gradient elution) to afford the title compound (32) (0.763 g, 86%); m/z 288 (M+H)+, (ES+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299073B2
Source datasetuspto-grants-2012_10
ORD IDord-84e8f4e18d3448bebabab9f732efd8a8
Source noteuspto-grants-2012_10