HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromo-5,5-dimethylhydantoin → HCID 14563110, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromo-5,5-dimethylhydantoin | HCID 6479 | — |
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | Chrysophanol dimethyl ether | HCID 189763 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 14563110 | HCID 14563110 | 95% |
Reaction Steps
To a hot solution of 1,8-dimethoxy-3-methyl-9,10-anthraquinone (4.5 g, 16 mM) and 1,3-dibromo-5,5-dimethylhydantoin (2.75 g, 19.2 mM) in carbon tetrachloride (500 mL) is added benzoyl peroxide (0.7 g), and the mixture is heated under reflux for 5 hours. The mixture is allowed to cool to room temperature. Insoluble hydantoin is removed by filtration, the filtrate is concentrated to dryness, and the residue recrystallized twice from ethyl acetate to give 3-bromomethyl-1,8-dimethoxy-9,10-anthraquinone (3.3 g, 57%), mp 176-178° C. 1H NMR (CDCl3) δ: 4.01 (3H, s, OMe), 4.03 (3H, s, OMe), 4.52 (2H, s, CH2Br), 7.26-7.84 (5H, m, aromatic H). Analyses (C17H13BrO4). Calculated: C, 56.53; H, 3.63; Br, 22.12. Found: C, 56.48; H, 3.67; Br, 21.93.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04966918 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-f5619eb70196410898118fe2bd7c11d9 |
| Source note | uspto-grants-1990_10 |