HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Amino-4-hydroxyanthraquinone → 1-Amino-2-bromo-4-hydroxyanthraquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Amino-4-hydroxyanthraquinone | HCID 8323 | — |
| Reactant | 1-Amino-2-bromoanthraquinone | HCID 236895 | — |
| Reactant | 1-Amino-4-bromoanthraquinone | HCID 627326 | — |
| Solvent | 1-Amino-2-hydroxyanthra-9,10-quinone | HCID 3478173 | — |
| Product | 1-Amino-2-bromo-4-hydroxyanthraquinone | HCID 8320 | — |
Reaction Steps
The progress of the bromination may be followed by thin layer chromatography or high pressure liquid chromatography so as to insure that the byproducts, 1-amino-2-bromoanthraquinone and 1-amino-4-bromoanthraquinone, represent less than 1% of the product mixture. This is essential, since hydroxylation of these two products results in 1-amino-2-hydroxyanthraquinone and 1-amino-4-hydroxyanthraquinone respectively. Both products are isolated along with the desired 1-amino-2-bromo-4-hydroxyanthraquinone and therefore give rise to a product with unsatisfactory quality.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04235789 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-323b5bf544664fefa041dc236dcb1427 |
| Source note | uspto-grants-1980_11 |