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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246663Generated: October 30, 2026

O-Methylhydroxylamine → HCID 178502860, compound

https://huagongshe.com/reaction/1246663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-MethylhydroxylamineHCID 4113—
Reactant4-(Azidomethyl)benzonitrileHCID 11073691—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventTriethylamineHCID 8471—
ProductHCID 178502860HCID 178502860—

Reaction Conditions

Temperature-10 °C

Reaction Steps

4-Azidomethylbenzonitrile (17.3 g, 0.109 mol; Nishiyama et al; Chem. Lett. (1982) 1477) was dissolved in 500 mL of toluene and 200 mL of absolute ethanol. The solution was cooled to −10° C. and HCl(g) was bubbled through until saturation. The mixture was kept in the refrigerator for 2 days when most of the solvents were evaporated. Diethyl ether was added and was decanted off. The product was re-dissolved in a solution of O-methylhydroxyl amine (10.5 g, 0.125 mol) and triethyl amine (56 mL) in 200 mL of methanol. The mixture was allowed to stand for 3 days whence the methanol was evaporated with addition of EtOAc. The organic phase was washed with water, dilute HOAc and aqueous sodium bicarbonate, dried (Na2SO4) and diluted with more EtOAc to a total volume of 500 mL.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129233B2
Source datasetuspto-grants-2006_10
ORD IDord-4b62ca25a18445cca3f8bb71f4f5cd6b
Source noteuspto-grants-2006_10