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HRID 650616作成日:2026年10月24日

2-(4,4-Difluorobut-3-enylthio)benzthiazole → 2-(4,4-Difluorobut-3-enylsulfonyl)benzthiazole

https://huagongshe.com/ja/reaction/650616

反応式

関与物質

役割名称HCID仕込み量
反応物2-(4,4-Difluorobut-3-enylthio)benzthiazoleHCID 21712909—
反応物Magnesium monoperoxyphthalic acid hexahydrateHCID 86597096—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物2-(4,4-Difluorobut-3-enylsulfonyl)benzthiazoleHCID 21712906—

反応手順

2-(4,4-difluorobut-3-enylthio)benzthiazole (prepared by the method described in United Kingdom Patent Application GB2270689A, 8.25 g) in dichloromethane ( 15 cm3) was added to a rapidly stirred mixture of monomagnesium peroxyphthalic acid hexahydrate (25.7 g, 70-80% technical grade) in water (25 cm3). The mixture was stirred for 2 days, diluted with dichloromethane and water, the organic phase separated, washed with aqueous sodium carbonate, water and dried (magnesium sulfate). The solvent was evaporated under reduced pressure to give 2-(4,4-difluorobut-3-enylsulfonyl )benzthiazole as a colourless oil, 4.9 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06274632B1
出典データセットuspto-grants-2001_08
ORD IDord-239314f354524ad9b811097d7640845e
出典メモuspto-grants-2001_08