HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 5-Bromo-2,6-diphenylpyrimidin-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,6-Diphenylpyrimidin-4-ol | HCID 135475560 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-Bromo-2,6-diphenylpyrimidin-4-ol | HCID 135467432 | 48.3% |
Reaction Steps
To a suspension of 13.37 g (56 mmol) of 2,6-diphenyl-4(3H)-pyrimidinone and 200 mL glacial acetic acid was added 15.1 g (84.8 mmol) of N-bromosuccinimide and the mixture was left to stir at room temperature for 60 h. The reaction was poured onto 100 g crushed ice and vacuum filtered, washing well with water, then air dried to yield 8.85 g (48%) 5-bromo-2,6-diphenyl-4(3H)-pyrimidinone, as a white solid. 1H-NMR (d6DMSO) δ 7.55(6H,m); 7.75(2H,m); 8.15(2H,m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05726124 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-f05000905bc748e98487d679b80f953b |
| Source note | uspto-grants-1998_03 |