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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1633739생성일: 2026년 10월 24일

Benzoyl Peroxide → 4-[(6-Acetoxyhexyl)sulfonyl]benzyl bromide

https://huagongshe.com/ko/reaction/1633739

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl PeroxideHCID 7187—
반응물N-bromobutanimideHCID 67184—
반응물4-[(6-Acetoxyhexyl)sulfonyl]tolueneHCID 18680025—
용매Carbon tetrafluorideHCID 6393—
생성물4-[(6-Acetoxyhexyl)sulfonyl]benzyl bromideHCID 1868002171%

반응 단계

2.0 g of 4-[(6-acetoxyhexyl)sulfonyl]toluene, 1.3 g of N-bromo-succinimide (NBS), 0.015 g of benzoyl peroxide (BPO) , and 20 mL of carbon tetrafluoride were added to a 250 mL round bottomed flask and heated with reflux for 12 hours in nitrogen. The mixture was allowed to cool down and then filtered. The filtrate was washed by deionized water repeatedly. The organic fraction was dried over anhydrous magnesium sulfate and then concentrated by a rotary evaporator. The concentrate was further purified by re-crystallization to produce a white solid. The yield was 71% with the following structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06503998B2
출처 데이터셋uspto-grants-2003_01
ORD IDord-d625cb0354ea4fdb9c0c5ba8db793974
출처 메모uspto-grants-2003_01