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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (2-Methoxy-6-methylbenzyl)phthalimide | HCID 21985073 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | (6-(Bromomethyl)-2-methoxybenzyl)phthalimide | HCID 21985106 | 86.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06734191B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-c036528d961546c299151d8f31fcc69f |
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| Source note | uspto-grants-2004_05 |
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