Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711737Generated: October 30, 2026

Hydrochloric Acid → 2-Amino-6-nitrobenzonitrile

https://huagongshe.com/reaction/711737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantDinitrobenzonitrileHCID 520718—
CatalystIronHCID 23925—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
Product2-Amino-6-nitrobenzonitrileHCID 1271572968.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

Concentrated HCl (39 mL) was added to a solution of 2,6-dinitrobenzonitrile (11.3 g, 58.5 mmol) in MeOH (235 mL) and 1,4-dioxane (145 mL) at 70° C. External heating was removed, and iron powder (11.44 g, 205 mmol) was added slowly in portions at a rate which maintained a temperature of 70° C. After the addition of iron was complete, the reaction was heated at reflux for a further 30 min, then cooled to room temperature and poured into EtOAc (400 mL) and water (400 mL). The solids were filtered out and extracted twice with boiling EtOAc (300 mL). The combined organic extract was dried with MgSO4, filtered and evaporated to give 2-amino-6-nitrobenzonitrile (6.5 g, 68%) as a red solid, which was used without further purification. 1H-NMR (400 MHz, DMSO-d6) δ 7.48-7.54 (m, 1H), 7.41-7.45 (m, 1H), 7.18-7.22 (m, 1H), 6.74 (broad s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181276B2
Source datasetuspto-grants-2015_11
ORD IDord-a83bd4e77f7343d4a6cd3f8be6790e57
Source noteuspto-grants-2015_11