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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735738Generated: October 31, 2026

N-bromobutanimide → Methyl 4-(bromomethyl)-3-methoxybenzoate

https://huagongshe.com/reaction/735738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantBenzoic acid, 3-methoxy-4-methyl-, methyl esterHCID 591123—
CatalystAzobisisobutyronitrileHCID 6547—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-(bromomethyl)-3-methoxybenzoateHCID 275982892%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592453B2
Source datasetuspto-grants-2009_09
ORD IDord-3deb605395dd496fb8ad683a39848389
Source noteuspto-grants-2009_09