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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27677Generated: October 27, 2026

Formamide → Acetamide, N-(2-(2-(2-cyano-4,6-dinitrophenyl)diazenyl)-5-(diethylamino)phenyl)-

https://huagongshe.com/reaction/27677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
ReactantAcetic AnhydrideHCID 7918—
ReactantAcetamide, N-[2-[2-(2-bromo-4,6-dinitrophenyl)diazenyl]-5-(diethylamino)phenyl]-HCID 104287—
ReactantSodium AcetateHCID 517045—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventButyl AcetateHCID 31272—
ProductAcetamide, N-(2-(2-(2-cyano-4,6-dinitrophenyl)diazenyl)-5-(diethylamino)phenyl)-HCID 9038388%

Reaction Conditions

Temperature110 °C

Reaction Steps

2-Bromo-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino) azobenzene (479 parts), copper (I) iodide (19 parts), anhydrous sodium acetate (246 parts), formamide (180 parts), acetic anhydride (408 parts) and n-butyl acetate (2190 parts) are mixed together and heated, with stirring, to 110° C. during 15 minutes. The temperature is maintained at 110° for 30 to 50 minutes, when a solid is suddenly precipitated from the reaction mixture, indicating completion of the reaction. The mixture is allowed to cool to room temperature and the product is collected, washed with ethanol to remove residual n-butyl acetate and dried. 2-Cyano-4,6-dinitro-2'-acetylamino-4'-(N,N-diethylamino)azobenzene is obtained in 88% yield and requires no purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04222935
Source datasetuspto-grants-1980_09
ORD IDord-79b9351e6cbc4c129c78b56e06bd30c6
Source noteuspto-grants-1980_09