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HRID 352396作成日:2026年10月27日

Water → 4-(Benzyloxy)benzene-1-sulfonyl chloride

https://huagongshe.com/reaction/352396

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ethyl AcetateHCID 8857—
反応物Thionyl ChlorideHCID 24386—
反応物Benzyl Phenyl EtherHCID 70352—
溶媒1,2-DichloroethaneHCID 11—
生成物4-(Benzyloxy)benzene-1-sulfonyl chlorideHCID 4738385—

反応手順

To a suspension of 22.4 g (146 mmol) of sulfur trioxide/DMF complex in 60 mL of anhydrous 1,2-dichloroethane at room temperature, was added a solution of 30 g (162 mmol) of benzylphenyl ether in 30 mL of anhydrous 1,2-dichloroethane. The resulting mixture was warmed to reflux and maintained there for 1 hour, cooled to room temperature and 10.8 mL (146 mmol) of thionyl chloride added. The reaction was then warmed to 75 C for 1 hour, cooled in an ice bath, 50 mL of water slowly added, then ethyl acetate. The layers were separated, washed with saturated sodium bicarbonate, brine, dried with magnesium sulfate, filtered and stripped. The resulting solids were triturated with hexane to afford 24.5 g of pure 4-(Benzyloxy)benzenesulfonyl chloride.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06747027B1
出典データセットuspto-grants-2004_06
ORD IDord-be569f83d1ea421887b5ea785b7a15d0
出典メモuspto-grants-2004_06