HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 5-Bromo-2-(bromomethyl)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-Bromo-2-methylpyrimidine | HCID 14387744 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 5-Bromo-2-(bromomethyl)pyrimidine | HCID 20557797 | 48% |
Reaction Steps
A mixture of 5-bromo-2-methylpyrimidine (100 mg, 0.58 mmol), NBS (103 mg, 0.58 mmol), dibenzoyl peroxide (10 mg, 0.04 mmol) in tetrachloromethane (10 mL) was refluxed for 36 h. The solvent was removed in vacuo and the residue was purified by column chromatography on silica gel (ethyl acetate in petroleum ether, 1% v/v) to give 5-Bromo-2-(bromomethyl)pyrimidine (70 mg, 48%) as a white solid. 1HNMR (400 MHz, CDCl3) δ 4.49 (s, 2H), 8.72 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08461157B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-baae7a979bc3473ea1959598bfcadcce |
| Source note | uspto-grants-2013_06 |