HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026195Generated: November 3, 2026
Ammonia → 4-Amino-3-nitrobenzimidamide hydrochloride
https://huagongshe.com/reaction/1026195
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ethyl 4-amino-3-nitrobenzimidate hydrochloride | HCID 67073287 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Amino-3-nitrobenzimidamide hydrochloride | HCID 67356092 | — |
Reaction Steps
4-Amino-3-nitro-benzimidic acid ethyl ester hydrochloride (84.5 g, 344 mmol) was suspended in absolute ethanol (750 mL) and then cooled to 0° C. Ammonia was then passed through the solution for a period of 2 h. The flask was tightly sealed and allowed to warm up to room temperature over an 18 h period with stirring. The product was crystallized with diethyl ether and the resulting solid was filtered, washed and dried to give 4-amino-3-nitrobenzamidine monohydrochloride (70.7 g) as an off-white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729117B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-99adb2c69d1d4314ae82acaf4db812f9 |
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| Source note | uspto-grants-2014_05 |
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