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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8905Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/8905

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl PeroxideHCID 7187—
EduktN-bromobutanimideHCID 67184—
Edukt(2-Methoxy-6-methylbenzyl)phthalimideHCID 21985073—
LösungsmittelDiethyl EtherHCID 3283—
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 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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091217B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-5c6876f3a159419d84868a80768d6864
Quellennotizuspto-grants-2006_08