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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1582245Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/1582245

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl PeroxideHCID 7187—
EduktN-bromobutanimideHCID 67184—
Edukt(2-Methoxy-6-methylbenzyl)phthalimideHCID 21985073—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt(6-(Bromomethyl)-2-methoxybenzyl)phthalimideHCID 2198510686,9%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06734191B2
Quelldatensatzuspto-grants-2004_05
ORD IDord-c036528d961546c299151d8f31fcc69f
Quellennotizuspto-grants-2004_05