Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cyclohexene | HCID 8079 | — |
| Reactant | Nitrogen oxide (N2O4) | HCID 25352 | — |
| Reactant | HCID 22761703 | HCID 22761703 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 21320324 | HCID 21320324 | — |
Reaction Steps
A mixture of 20 g (0.063 mole) of 2-bromo-3-phenyl-5-benzofurancarboxylic acid and 1.25 l of acetic acid is stirred and heated to 55° C. To this mixture is added 7.7 g (0.094 mole) of cyclohexene. To this mixture is added dropwise 8.7 g (0.094 mole) of dinitrogen tetroxide in 25 ml of acetic acid. After 5 hours the mixture is poured into cold water and the solid product is collected. Recrystallization from aqueous ethanol followed by recrystallization from a benzene-ethanol mixture provides 2-nitro-3-phenyl-5-benzofurancarboxylic acid, m.p. 271°-273° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04067993 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-f59f405228fb4f9a9ddfe10cb8331615 |
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| Source note | uspto-grants-1978_01 |
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