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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770254Generated: November 4, 2026

Hydrochloric Acid → HCID 178424372, compound

https://huagongshe.com/reaction/1770254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNitrogenHCID 947—
ReactantSodium HydroxideHCID 14798—
ReactantSodium AzideHCID 33557—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 178424371HCID 178424371—
SolventWaterHCID 962—
ProductHCID 178424372HCID 178424372—

Reaction Steps

N-(2-Methylphenyl)-N'-(2-methyl-4-aminophenyl)guanidine dihydrochloride (112 mg, 0.341 mmol) were dissolved in 2 ml H2O and 100 ul conc. HCl (1.2 mmol). The solution was cooled in an ice bath, and a solution of NaNO2 (42 mg, 0.61 mmol) in 450 ul H2O were added. The reaction mixture turned yellow, and was stirred for 45 min before solid NaN3 (43 mg, 0,661 mmol) was added in a single portion. After N2 evolution was caused, a foamy solid (11 mg) was removed and discarded. Solid NaOH (96 mg, 2.41 mmol) was added, and the bright yellow precipitate was extracted with Et2O (3×5 ml). Evaporation of the combined Et2O layers gave a yellow solid which was crystallized from EtOH/H2O: NMR (CD3OD) 2.279 (s, 3H), 2.284 (s, 3H), 6.864 (dd, 1H, J=2.4 Hz, 8.4 Hz), 6.914 (d, 1H, J=2.1 Hz), 7.055 (td, 1H, J=1.8 Hz, 7.2 Hz), 7.136-7.229 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05385946
Source datasetuspto-grants-1995_01
ORD IDord-16e87a6ec5d141c8b8abda8e51ccf77d
Source noteuspto-grants-1995_01