HuagongsheHuagongshe Chemistry Print Report · For research reference only
Anthraquinone → 9,10-Anthracenediol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Anthraquinone | HCID 6780 | — |
| Reactant | Disodium | HCID 141233 | — |
| Reactant | 1,5-Anthraquinone disulfonic acid | HCID 53420095 | — |
| Product | 9,10-Anthracenediol | HCID 21082 | — |
Reaction Steps
The anthraquinone model compound (1,5-anthraquinonedisulfonic acid, disodium salt) and two polymers were subjected to the hydrogenation conditions. The reaction mixtures were analyzed with UV/visible spectroscopy following removal of the catalyst under an inert atmosphere (argon or nitrogen). Where anthrahydroquinone is formed, a bright yellow solution results. The results of some of the hydrogenation experiments are determined from the absorption spectra both before and after hydrogenation, and are summarized in Table 4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05624543 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-3950b6f93eb54f19842ce2fa60356bc9 |
| Source note | uspto-grants-1997_04 |