HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712933Generated: October 30, 2026
Hydrochloric Acid → Ethyl 4-amino-3-nitrobenzimidate hydrochloride
https://huagongshe.com/reaction/712933
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Amino-3-nitrobenzonitrile | HCID 595901 | — |
| Reactant | Ethyl 4-amino-3-nitrobenzimidate | HCID 53872271 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl 4-amino-3-nitrobenzimidate hydrochloride | HCID 67073287 | — |
Reaction Steps
A mixture of 4-amino-3-nitrobenzonitrile (63.3 g, 388 mmol) in 1,4-dioxane (600 mL) and anhydrous ethanol (600 mL) was cooled in an ice water bath to 0-5° C. and treated with gaseous HCl for 1.5 h. The reaction mixture was tightly sealed and allowed to warm up to room temperature with stirring for 18 h. The flask was then carefully unsealed and the reaction mixture was diluted with anhydrous diethyl ether (about 2.4 L) until a cloudy solution was obtained. A minimum amount of absolute ethanol required to give a clear solution was then added, and the resulting solution stirred until crystals of 4-amino-3-nitro-benzimidic acid ethyl ester were observed. Ether was then cautiously added to complete the crystallization process and the suspension was allowed to stand for about 30 minutes. The crystals were filtered and washed with dry diethyl ether, then allowed to dry under aspirator vacuum. The crystals were dried in vacuo to give 4-amino-3-nitro-benzimidic acid ethyl ester hydrochloride (84.6 g) as off-white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181280B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-bbe581a8ae7e409caf6629e36a1adfe9 |
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| Source note | uspto-grants-2015_11 |
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