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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8905생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl PeroxideHCID 7187—
반응물N-bromobutanimideHCID 67184—
반응물(2-Methoxy-6-methylbenzyl)phthalimideHCID 21985073—
용매Diethyl EtherHCID 3283—
생성물(6-(Bromomethyl)-2-methoxybenzyl)phthalimideHCID 2198510686.9%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091217B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-5c6876f3a159419d84868a80768d6864
출처 메모uspto-grants-2006_08