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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157885Generated: November 4, 2026

N-bromobutanimide → Ethyl 2-bromomethyl-6-methoxybenzoate

https://huagongshe.com/reaction/1157885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Methoxy-6-methyl-benzoic acid ethyl esterHCID 591060—
CatalystBenzoyl PeroxideHCID 7187—
SolventDiethyl EtherHCID 3283—
SolventCarbon TetrachlorideHCID 5943—
ProductEthyl 2-bromomethyl-6-methoxybenzoateHCID 1003892660%

Reaction Steps

To a solution of ethyl 2-methoxy-6-methylbenzoate (0.813 g, 4.19 mmol) in CCl4 (8 mL) was added recrystallized N-bromosuccinimide (0.751 g, 4.22 mmol) followed by benzoyl peroxide (52 mg, 0.22 mmol). The resultant mixture was heated to reflux for 90 minutes then cooled to room temperature. The mixture was diluted with diethyl ether (50 mL), filtered through filter paper, and the filtrate was concentrated. Purification of the crude material by column chromatography (8:1 hexanes-EtOAc) provided 0.68 g (60%) of ethyl 6-(bromomethyl)-2-methoxybenzoate as a colorless oil. 1H NMR (CDCl3) δ 1.42 (t, 3H, J=7.2 Hz), 3.84 (s, 3H), 4.45 (q, 2H, J=7.2 Hz), 4.50 (s, 2H), 6.89 (d, 1H, J=8.4 Hz), 7.01 (d, 1H, J=7.2 Hz), 7.34 (dd, 1H, J=7.2, 8.4 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807694B2
Source datasetuspto-grants-2010_10
ORD IDord-b67b8b87918e446794734aba24cdeada
Source noteuspto-grants-2010_10