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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612186Generated: November 2, 2026

Hydrogen Peroxide → Ammonium Hydroxide

https://huagongshe.com/reaction/1612186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantAcetonitrileHCID 6342—
ReactantMethyl trifluoromethyl ketoneHCID 9871—
Reactant1,2-DihydronaphthaleneHCID 9938—
SolventPotassium CarbonateHCID 11430—
ProductAmmonium HydroxideHCID 149230.5%
Product(1R,2R)-1-Amino-1,2,3,4-tetrahydronaphthalen-2-olHCID 13125680—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 1,2-dihydronaphthalene (5.12 g) and trifluoroacetone (1.34 g) in acetonitrile (60 ml) and aqueous potassium carbonate (1.5M in 0.4 mM EDTA, 60 ml) was added H2O2 (30%, 18.2 ml) at 0° C. Upon stirring at 0° C. for 4 hours, the rxn mixture was extracted with Et2O, washed with aqueous Na2S2O3 (1M) and brine, dried (MgSO4), filtered and concentrated. The epoxide was used without purification. A mixture of 1a,2,3,7b-tetrahydronaphtho[1,2-b]oxirene and ammonium hydroxide was stirred at 40° C. for 3 days. The excess solvent was removed in vacuo. Flash chromatography (Silica gel, 1:20 MeOH:CH2Cl2, 0.5% NH4OH) gave the title compound. HRMS (FAB) calcd for C10H13NO+H 164.1075, found 164.1075.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06992087B2
Source datasetuspto-grants-2006_01
ORD IDord-5428017c805141bbb70df1eba1411897
Source noteuspto-grants-2006_01