HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658866Generated: November 1, 2026
HCID 178418361, compound → 1-Aminoanthraquinone
https://huagongshe.com/reaction/1658866
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178514954 | HCID 178514954 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 1-Aminoanthraquinone | HCID 6710 | — |
Reaction Steps
To 100 parts of ethyleneglycol monomethyl ether (so called methyl-Cellosolve) there were added 5.0 parts of 1-hydroxylaminoanthraquinone and 0.25 part of Raney nickel. The reaction mixture was heated to 80°C over 30 minutes and maintained at 80°C for 4 hours, with stirring, while introducing thereinto 0.04 parts/hour of gaseous hydrogen. The reaction mixture was then purged of gaseous hydrogen with gaseous nitrogen, heated to 100°C and filtered while hot to separate the catalyst as residue. The filtrate was, while maintained at 80°C, added with 100 parts of water, with stirring, to precipitate crystals. The slurry thus formed was then cooled to room temperature and filtered. The residue was washed with 5 parts of methanol and dried to obtain 4.2 parts of 1-aminoanthraquinone of a purity of 97 %. In the filtrate there remained 0.1 part of 1-aminoanthraquinone dissolved.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03966775 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-f42cafdf3ffe4cdc823468fe0469ad6a |
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| Source note | uspto-grants-1976_06 |
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