Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Methyl trifluoromethyl ketone | HCID 9871 | — |
| Reactant | 1,2-Dihydronaphthalene | HCID 9938 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | Ammonium Hydroxide | HCID 14923 | 0.5% |
| Product | (1R,2R)-1-Amino-1,2,3,4-tetrahydronaphthalen-2-ol | HCID 13125680 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06992087B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-5428017c805141bbb70df1eba1411897 |
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| Source note | uspto-grants-2006_01 |
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