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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8905Generated: October 26, 2026

Benzoyl Peroxide → (6-(Bromomethyl)-2-methoxybenzyl)phthalimide

https://huagongshe.com/reaction/8905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant(2-Methoxy-6-methylbenzyl)phthalimideHCID 21985073—
SolventDiethyl EtherHCID 3283—
Product(6-(Bromomethyl)-2-methoxybenzyl)phthalimideHCID 2198510686.9%

Reaction Steps

To a solution of (2-methoxy-6-methylbenzyl)phthalimide (0.286 g, 1.02 mmol) in CC4 (25 mL) was added recrystallized N-bromosuccinimide (0.177 g, 0.99 mmol) followed by benzoyl peroxide (28 mg, 0.11 mmol). The resultant mixture was heated to reflux for 90 minutes then cooled to room temperature. The mixture was diluted with diethyl ether (25 mL), filtered through filter paper, and the filtrate was concentrated. Purification of the crude material by column chromatography (3:1 hexanes-EtOAc) provided 0.31 g (86%) of (6-(bromomethyl)-2-methoxybenzyl)phthalimide as a white solid. 1H NMR (CDCl3) δ 3.78 (s, 3H), 4.90 (s, 2H), 5.00 (s, 2H), 6.83 (d, 1H, J=8.4 Hz), 6.98 (d, 1H, J=7.2 Hz), 7.25 (dd, 1H, J=7.2, 8.4 Hz), 7.67–7.69 (m, 2H), 7.78–7.81 (m, 2H). ES-MS m/z 382 (M+Na), 384 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091217B2
Source datasetuspto-grants-2006_08
ORD IDord-5c6876f3a159419d84868a80768d6864
Source noteuspto-grants-2006_08