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HRID 1182749作成日:2026年10月26日

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

https://huagongshe.com/reaction/1182749

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US08664227B2
出典データセットuspto-grants-2014_03
ORD IDord-c05f0c0217764d12a28a8c9a9031236d
出典メモuspto-grants-2014_03