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HRID 1633739作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl PeroxideHCID 7187—
反応物N-bromobutanimideHCID 67184—
反応物4-[(6-Acetoxyhexyl)sulfonyl]tolueneHCID 18680025—
溶媒Carbon tetrafluorideHCID 6393—
生成物4-[(6-Acetoxyhexyl)sulfonyl]benzyl bromideHCID 1868002171%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06503998B2
出典データセットuspto-grants-2003_01
ORD IDord-d625cb0354ea4fdb9c0c5ba8db793974
出典メモuspto-grants-2003_01