Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 57297197 | HCID 57297197 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86740031 | HCID 86740031 | — |
Reaction Steps
35 parts of 30 percent strength aqueous H2O2 were added dropwise, in the course of 1 hour, to 50 parts of 8-(4-bromophenyl)-12-hydroxy-3,4,8,9,10-pentazatetracyclo[5,4,1,02,5,07,11 ]dodec-9ene (Compound No. 69) in 400 parts of methanol and 5 parts of 25 percent strength by weight aqueous NaOH, at 65° C., while stirring, and stirring was continued for 5 hours at 65° C. The mixture was cooled to 20° C., after which 1,500 parts of water were added, and the product was filtered off under suction, washed with 300 parts of water and dried at 30° C. under 1 mbar. 44 parts (88 mole %) of 8-(4-bromophenyl)-12hydroxy-3,4,8,9,10-pentazatetracyclo[5,4,1,02,5,07,11 ]-dodeca-3,9-diene of melting point 187° C. (decomposition) were obtained (Compound No. 3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04512795 |
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| Source dataset | uspto-grants-1985_04 |
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| ORD ID | ord-7fb0b012a612421d8d40a5bc8ba4a2c0 |
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| Source note | uspto-grants-1985_04 |
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