HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073178Generated: October 30, 2026
Acetamidine monohydrochloride → HCID 15087820, compound
https://huagongshe.com/reaction/1073178
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetamidine monohydrochloride | HCID 67170 | — |
| Reactant | 3-(Phenylazo)-2,4-pentanedione | HCID 91785 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15087820 | HCID 15087820 | 13.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04968684 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-a353c8f8a4284091bcbcd8d3df1569ed |
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| Source note | uspto-grants-1990_11 |
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