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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-methoxy-5-methylbenzoateHCID 10241396—
CatalystBenzoyl PeroxideHCID 7187—
SolventAcetonitrileHCID 6342—
ProductMethyl 5-(bromomethyl)-2-methoxybenzoateHCID 1974434044%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365553B2
Source datasetuspto-grants-2016_06
ORD IDord-363618aa9b0c4c0fa230acbfc2a2d92c
Source noteuspto-grants-2016_06