Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582245Generated: October 25, 2026

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

https://huagongshe.com/reaction/1582245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant(2-Methoxy-6-methylbenzyl)phthalimideHCID 21985073—
SolventDiethyl EtherHCID 3283—
SolventCarbon TetrachlorideHCID 5943—
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 CCl4 (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) δ3.78 (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 numberUS06734191B2
Source datasetuspto-grants-2004_05
ORD IDord-c036528d961546c299151d8f31fcc69f
Source noteuspto-grants-2004_05