HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 2-Methoxyphenyl 2-methoxy-3-bromomethylphenyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Methoxyphenyl 2-methoxy-3-methylphenyl ether | HCID 13066656 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Methoxyphenyl 2-methoxy-3-bromomethylphenyl ether | HCID 13066657 | 101.6% |
Reaction Steps
N-Bromosuccinimide (6.56 g) and 2,2'-azobisisobutyronitrile (100 mg) were added to a solution of 2-methoxyphenyl 2-methoxy-3-methylphenyl ether (9.0 g) in benzene (100 ml), and the mixture was refluxed under heating for 2 hrs. The reaction mixture was evaporated, and water was added to the residue. The mixture was extracted with diethyl ether, and the extract was washed with water, dried over magnesium sulfate and then evaporated to give oily residue of 2-methoxyphenyl 2-methoxy-3-bromomethylphenyl ether (12.10 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04367238 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-04f85c56c26e4a01b2accc39660b98bd |
| Source note | uspto-grants-1983_01 |