Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 10035507 | HCID 10035507 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Benzofuroxan | HCID 68075 | 94.3% |
Reaction Steps
A mixture of the 4-methoxy-2-nitrophenylazide (5.06 g, 26.1 mmol) and 7.8 mL of fleshly distilled toluene was heated to 110° C. for three hours and then cooled to 95° C. and stirred for an additional two hours. The toluene was removed in vacuo to give a brown solid. The crude product was recrystallized from methanol to yield 3.35 g (77% yield) of benzofuroxan as orange-brown crystals (m.p. 114°-115° C.). Rf 0.30 in 20% ethyl acetate/hexane. 1HNMR (CDCl3) δ 6.19 7.45 (m, 3H), 3.89 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05637591 |
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| Source dataset | uspto-grants-1997_06 |
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| ORD ID | ord-ad4cbf9c067244cd9bc686cf42918f69 |
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| Source note | uspto-grants-1997_06 |
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