HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 2-[4-(Bromomethyl)-3-methoxyphenyl]-1,3-benzoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-(3-Methoxy-4-methylphenyl)-1,3-benzoxazole | HCID 21990968 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-[4-(Bromomethyl)-3-methoxyphenyl]-1,3-benzoxazole | HCID 21990991 | — |
Reaction Steps
2-(3-Methoxy-4-methylphenyl)-1,3-benzoxazole (1.0 g, 4.1 mmol), carbon tetrachloride (18 mL), benzoyl peroxide (66 mg, 0.3 mmol) and N-bromosuccinimide (970 mg, 5.4 mmol) was heated to reflux conditions under argon and placed under a UV light. After one hour, no starting material was observed by TLC. After cooling mixture to rt, filtered, washing with dichoromethane. After concentrating filtrate in vacuo, the resulting colorless solid was purified by flash chromatography, using a gradient elution of 1:4 EtOAc:hexanes to EtOAc. This afforded the desired intermediate, 2-[4-(bromomethyl)-3-methoxyphenyl]-1,3-benzoxazole, as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07087601B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-a804c7f51ce54084918ff23496b95166 |
| Source note | uspto-grants-2006_08 |