HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057952Generated: November 1, 2026
HCID 178418361, compound → HCID 178428576, compound
https://huagongshe.com/reaction/2057952
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178426129 | HCID 178426129 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178428576 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04213995 |
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| Source dataset | uspto-grants-1980_07 |
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| ORD ID | ord-11bdc2059c7747a1b39d632be0b5ec4e |
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| Source note | uspto-grants-1980_07 |
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