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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658040Generated: November 2, 2026

Hydrochloric Acid → HCID 136353538, compound

https://huagongshe.com/reaction/1658040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantUreaHCID 1176—
Reactant3-AminopyridineHCID 10009—
ReactantN-methylhydroxylamine hydrochlorideHCID 77906—
ReactantSodium AcetateHCID 517045—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductHCID 136353538HCID 136353538—

Reaction Steps

To a solution of 9.4 g. of 3-aminopyridine in 31 ml. of 12N hydrochloric acid and 250 ml. of water at 0° was added in small portions a solution of 7.0 g. of sodium nitrite in 12 ml. of water. After the mixture was stirred 30 minutes at 0°, 2.2 g. of urea was added, and the solution was stirred for 15 minutes. The solution was added in one portion to a mixture of 8.35 g. of N-methylhydroxylamine hydrochloride and 50 g. of sodium acetate in 80 ml. of water at about 0° to 5°C. The mixture was stirred over the weekend at 25°C. The reaction mixture was diluted with water and extracted with ethyl acetate three times. The pooled ethyl acetate extract was dried and concentrated to give a mixture of product and recovered 3-aminopyridine. The crude produce was chromatographed on 500 ml. of silica gel using benzene and ethyl acetate mixtures. Solid 1 -methyl-3-(3-pyridyl)triazene-1-oxide was obtained by concentration of the mixture of benzene and ethyl acetate from chromatographic elution. Recrystallization of the product from benzene by adding hexane gave 3.3 g. of crystals, m.p. 95°-97°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03962434
Source datasetuspto-grants-1976_06
ORD IDord-b31e29abcbd4403cb0451db487e5fb09
Source noteuspto-grants-1976_06