HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → Methyl 4-(bromomethyl)-3-methoxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Benzoic acid, 3-methoxy-4-methyl-, methyl ester | HCID 591123 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 4-(bromomethyl)-3-methoxybenzoate | HCID 2759828 | 92% |
Reaction Steps
A mixture of methyl 3-methoxy-4-methylbenzoate (10.0 g, 55.5 mmol), N-bromosuccinimide (10.7 g, 60.9 mmol), 2,2′-azobis(isobutyronitrile) (1.6 mg) and ethyl acetate (200 ml) was heated under reflux overnight. The solvent was evaporated under reduced pressure, and hexane was added to the residue. The precipitate was filtered off, and the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and eluted with hexane-ethyl acetate (9:1-7:3, v/v) to give the title compound (12.8 g, 92%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943770B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-9219d7bcbb6344ff8739695759bb3299 |
| Source note | uspto-grants-2011_05 |