HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 4-(3-Bromomethyl-5-methyl-phenoxy)-2,6-dichloro-5-isopropyl-pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,4-Dichloro-6-(3,5-dimethyl-phenoxy)-5-isopropyl-pyrimidine | HCID 18925252 | — |
| Catalyst | Tungsten | HCID 23964 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-(3-Bromomethyl-5-methyl-phenoxy)-2,6-dichloro-5-isopropyl-pyrimidine | HCID 59184689 | 66.2% |
Reaction Steps
A mixture of (65) (9.72 g, 31 mmol), NBS (5.56 g, 31 mmol), and benzoyl peroxide (0.756 g, 3.1 mmol) in carbon tetrachloride (60 ml) was refluxed for 3 hr. under a light of 500 W tungsten lamp. After cooling to room temperature, the reaction mixture was filtered and evaporated in vacuo. The residue was purified by silica gel column chromatography (eluent, ether:hexanes (1:19)) to afford 8 g (62%) of a white solid. m.p. 98-101° C.; 1H NMR (200 MHz, CDCl3) δ 1.41 (6H, d, J=7.2 Hz), 2.38 (3H, s), 3.59 (1H, m), 4.47 (2H, s), 6.86 (1H, s), 6.97 (1H, s), 7.13 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106064B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-726e6e4fd00c4b62a277228d14ad4316 |
| Source note | uspto-grants-2012_01 |