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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8943Generated: October 26, 2026

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

https://huagongshe.com/reaction/8943

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 numberUS07091217B2
Source datasetuspto-grants-2006_08
ORD IDord-f64e217233764463aa5656221e71fb06
Source noteuspto-grants-2006_08