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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961492Generated: October 31, 2026

Hydrochloric Acid → Ethyl 4-amino-3-nitrobenzimidate hydrochloride

https://huagongshe.com/reaction/1961492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Amino-3-nitrobenzonitrileHCID 595901—
ReactantEthyl 4-amino-3-nitrobenzimidateHCID 53872271—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 4-amino-3-nitrobenzimidate hydrochlorideHCID 67073287—

Reaction Conditions

Temperature2.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415328B2
Source datasetuspto-grants-2013_04
ORD IDord-f1cecd949c21491bb75523cffa0ccbe7
Source noteuspto-grants-2013_04