Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | C.I. Pigment Orange | HCID 25535 | — |
| Reactant | p-Amino-n-ethylpyridinium bromide | HCID 13073421 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzimidazol-2-one | HCID 162542 | — |
Reaction Steps
20 parts of abenzimidazolone orange pigment (C.I. pigment orange 36) which had been previously finely ground and 62 parts of p-amino-N-ethylpyridinium bromide were dispersed in 150 parts of water. To the mixture were then added dropwise 32 parts of nitric acid. The mixture was then stirred at a temperature of 75° C. for 5 minutes. To the mixture was then added an aqueous solution of sodium nitrite. The mixture was further stirred for 2 hours, and then repeatedly rinsed and filtered to obtain a slurry of a surface-treated benzimidazolone orange pigment having an N-ethylpyridyl group introduced therein with the interposition of phenyl group.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06916862B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-0585871de8ee4d9eb9d87c52fda35eca |
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| Source note | uspto-grants-2005_07 |
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