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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073178Generated: October 30, 2026

Acetamidine monohydrochloride → HCID 15087820, compound

https://huagongshe.com/reaction/1073178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamidine monohydrochlorideHCID 67170—
Reactant3-(Phenylazo)-2,4-pentanedioneHCID 91785—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductHCID 15087820HCID 1508782013.8%

Reaction Steps

To a stirred solution of 50 parts of 3-(phenylazo)-2,4-pentanedione and 35 parts of ethanimidamide monohydrochloride in 711 parts of ethanol was added a solution of 8.5 parts of sodium in 126 parts of ethanol. After stirring overnight at room temperature, the precipitate was filtered off and the filtrate was stirred for 2 days at room temperature. The mixture was evaporated and the residue was diluted with a sodium hydroxide solution 10%. The separated aqueous layer was extracted with methylbenzene. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (98:2 by volume) as eluent. The pure fractions were collected and the eluent was evaporated with methylbenzene, yielding 7.5 parts (13.8%) of 4,6-dimethyl-5-(phenylazo)-2-pyridinamine as a residue (int. 95).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968684
Source datasetuspto-grants-1990_11
ORD IDord-a353c8f8a4284091bcbcd8d3df1569ed
Source noteuspto-grants-1990_11