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HRID 447224作成日:2026年10月26日

Chlorobenzene → N'-[2-[4-(bromomethyl)phenyl]phenyl]sulfonyl-N,N-dimethylmethanimidamide

https://huagongshe.com/reaction/447224

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorobenzeneHCID 7964—
反応物N-bromobutanimideHCID 67184—
反応物N,N-dimethyl-N'-[2-(4-methylphenyl)phenyl]sulfonylmethanimidamideHCID 9972170—
触媒Benzoyl PeroxideHCID 7187—
溶媒WaterHCID 962—
生成物N'-[2-[4-(bromomethyl)phenyl]phenyl]sulfonyl-N,N-dimethylmethanimidamideHCID 1031768841%

反応条件

温度100 °C

反応手順

4′-Methylbiphenyl-2-sulfonic acid 1-dimethylaminometh-(E)-ylideneamide (540.0 mg, 1786 μmol), NBS (318 mg, 1.8 mmol), and benzoyl peroxide (4.3 mg, 17.8 μmol) were dissolved in chlorobenzene (7.0 mL, 69 mmol) and the resulting solution was heated at 100° C. for 90 minutes. The mixture was cooled to room temperature and water was added. The mixture was extracted with DCM, washed with saturated NaHCO3 and saturated aqueous NaCl, extracted again with DCM, dried over MgSO4, filtered, and concentrated. The crude product was purified by flash chromatography (40 g, 0-100% EtOAc in hexanes), then taken up in EtOAc (4.5 mL) and DCM (1.5 mL). Additional DCM (3.0 mL) was added and the mixture was heated at 60° C. The mixture was cooled in the freezer overnight, then concentrated. The material was taken up in DCM (2 mL), EtOAc (6 mL) was added, and the resulting solution placed in the freezer. A precipitate formed and was filtered to yield the title compound (279 mg) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481549B2
出典データセットuspto-grants-2013_07
ORD IDord-a0954227e54f42939031ea246f17d11f
出典メモuspto-grants-2013_07