HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202592Generated: October 25, 2026
N-bromobutanimide → Methyl 5-(bromomethyl)-2-methoxybenzoate
https://huagongshe.com/reaction/2202592
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 2-methoxy-5-methylbenzoate | HCID 10241396 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 5-(bromomethyl)-2-methoxybenzoate | HCID 19744340 | 44% |
Reaction Steps
Under a nitrogen atmosphere, methyl 2-methoxy-5-methylbenzoate (901 mg, 5 mmol) was dissolved in acetonitrile, and N-bromosuccinimide (890 mg, 5 mmol) and benzoyl peroxide (24 mg, 0.1 mmol) were added thereto. The mixture was refluxed for one hour. After the completion of the reaction was confirmed by HPLC, the reaction mixture was allowed to cool down to a room temperature, and the solvent was distilled off. Thereafter, the residue was dissolved in ethyl acetate. The organic layer was washed with water 3 times and then with a saturated saline solution, and dried over magnesium sulfate. The solvent was distilled off, and then the resulting residue was purified by flash column chromatography (Yamazen, Hi-Flash column, silica gel, hexane/ethyl acetate (volume ratio)=10:1) to give the title compound (570 mg, 44.0%) as an oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09365553B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-363618aa9b0c4c0fa230acbfc2a2d92c |
|---|
| Source note | uspto-grants-2016_06 |
|---|