Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Nitroanthraquinone | HCID 6704 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178514954 | HCID 178514954 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 1-Aminoanthraquinone | HCID 6710 | 97% |
Reaction Steps
300 Parts by weight of anisole are mixed with 27 parts of (97%) 1-nitroanthraquinone and 0.2 parts by weight of a palladium/charcoal catalyst (5% of Pd on active charcoal) and heated to 130° in an autoclave. At this temperature, hydrogen is blown through until the rate of up-take of the hydrogen has fallen to 10% of the original value. At this stage, about 2% of overhydrogenation product is present (ascertained by TLC). After interruption of the hydrogen supply, at 130°, 0.4 parts by weight of 1-hydroxylaminoanthraquinone are added and stirring is effected for 30 minutes. The catalyst is separated off at the upper temperature, the filtrate is concentrated and cooled and the 1-aminoanthraquinone is filtered off. No nuclear hydrogenated 1-aminoanthraquinone is present in the mother liquor. 23 Parts of 97% pure 1-aminoanthraquinone is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03966774 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-d7d4a0b142d3488c9fbcb1e21e30c0ce |
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| Source note | uspto-grants-1976_06 |
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