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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057952Generated: November 1, 2026

HCID 178418361, compound → HCID 178428576, compound

https://huagongshe.com/reaction/2057952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178426129HCID 178426129—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductHCID 178428576HCID 178428576—

Reaction Steps

3.05 gm (0.012 mol) of 2-(2-chloro-4-methyl-6-nitrophenylimino)-imidazolidine were hydrogenated in a shaker autoclave at 25°-30° C. and atmospheric pressure in the presence of Raney nickel and in a 1:1 mixture of methanol and tetrahydrofurn until the theoretical amount of hydrogen had been absorbed. Thereafter, the catalyst was separated by suction filtration, and the filtrate was evaporated in vacuo until the weight of the residue remained constant. Yield: 2.6 gm (96.5% of theory) of 2-(2-amino-6-chloro-4-methyl-phenylimino)-imidazolidine, an oily substance having an Rf -value of 0.3 in the mobile phase 50 parts benzene, 40 parts dioxane, 5 parts ethanol and 5 parts concentrated ammonium hydroxide; carrier: silicagel G; visualization: ultraviolet light and potassium iodoplatinate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04213995
Source datasetuspto-grants-1980_07
ORD IDord-11bdc2059c7747a1b39d632be0b5ec4e
Source noteuspto-grants-1980_07