Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonyl azide | HCID 13661 | — |
| Reactant | 2-Tetralone | HCID 68266 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 11084333 | HCID 11084333 | 12% |
Reaction Steps
To a solution of sodium ethoxide (20.0 g, 0.20 mole) in ethanol (600 ml), a solution of 2-tetralone (42.4 g, 0.29 mole) in ethanol (100 ml) was added dropwise at 0° C. with stirring, then p-toluenesulfonylazide (59.2 g, 0.3 mole) was added dropwise at -15° C. or below to the mixture and reacted with stirring for 3 hours at -10° to 0° C. The reaction mixture was poured into H2O (1 l), extracted with methylene chloride (500 ml×2), the organic layer separated was washed with H2O (500 ml×3), dried over anhydrous MgSO4 and evaporated. The oily residue (72 g) was chromatographed on silica gel (Wakogel C-200) with n-hexane-n-hexane/methylene chloride (1/1) as eluent and recrystallized from n-hexane to afford 6.0 g of 1-diazo-2-tetralone as yellow crystals. m.p. 42.5°-44.2° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05558971 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-19fb1ba979314da09e671ca9b56d6a52 |
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| Source note | uspto-grants-1996_09 |
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