HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071781Generated: October 26, 2026
Pyridine → N-{4[(acetyloxy)imino]-2,5-cyclohexadien-1-ylidene}aniline
https://huagongshe.com/reaction/1071781
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-Nitrosodiphenylamine | HCID 9074 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-{4[(acetyloxy)imino]-2,5-cyclohexadien-1-ylidene}aniline | HCID 20801492 | — |
Reaction Steps
A solution was prepared by mixing 4-nitrosodiphenylamine, 19.8 grams, (0.10 mole), pyridine, 8.6 grams, (0.11 mole), and toluene, 10 mL, in a suitable reaction flask. The solution was cooled to 5° C. and acetic anhydride, 11.22 grams, (0.11 mole) was added slowly. The mixture was stirred for 2 hours and allowed to come to room temperature. The reaction mixture was mixed with a quantity of water, allowed to stand until the water layer separated, and the water layer was discarded. The toluene solution was evaporated to leave 21.4 grams of a solid residue, 96% of theory. The material melted at 63-65° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06906121B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-ec5e0582668946a39c1d9a9f080e78be |
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| Source note | uspto-grants-2005_06 |
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