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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTolueneHCID 1140—
ReactantAcetic AnhydrideHCID 7918—
Reactant4-NitrosodiphenylamineHCID 9074—
SolventWaterHCID 962—
ProductN-{4[(acetyloxy)imino]-2,5-cyclohexadien-1-ylidene}anilineHCID 20801492—

Reaction Conditions

Temperature5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06906121B2
Source datasetuspto-grants-2005_06
ORD IDord-ec5e0582668946a39c1d9a9f080e78be
Source noteuspto-grants-2005_06