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HRID 2914作成日:2026年10月23日

Dichloromethane → Triphenylsulfonium 4-trifluoromethylbenzenesulfonate

https://huagongshe.com/ja/reaction/2914

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Sodium CarbonateHCID 10340—
反応物Triphenylsulfonium chlorideHCID 61343—
反応物4-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2777399—
溶媒WaterHCID 962—
生成物Triphenylsulfonium 4-trifluoromethylbenzenesulfonateHCID 22057398—

反応手順

A suspension of 4-trifluoromethylbenzenesulfonyl chloride (20.53 g, 83.9 mmol) in water (150 ml) containing sodium carbonate (9.43 g, 88.10 mmol) was heated at reflux for 22 hours. After cooling to room temperature, triphenylsulfonium chloride (50% aqueous solution, 50.00 g) was added over 15 minutes. After stirring the biphasic mixture for 30 minutes, dichloromethane (300 ml) was added and the mixture stirred at room temperature for 20 hours. The layers were separated and the organic layer washed with water (7×150 ml) until the washings were neutral (pH 7 ). After drying (MgSO4 ), removal of the solvent in vacuo gave a pale yellow foam which was further dried by heating at 80°-100° C. for 108 hours under vacuum. In this way, triphenylsulfonium 4 -trifluoromethylbenzenesulfonate was isolated as a pale yellow glass (36.77 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731364
出典データセットuspto-grants-1998_03
ORD IDord-36355329f50b4fba91d75f1d3bd8c47f
出典メモuspto-grants-1998_03