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HRID 219506作成日:2026年10月27日

Hydrochloric Acid → Triphenylsulfonium chloride

https://huagongshe.com/reaction/219506

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物ChlorotrimethylsilaneHCID 6397—
反応物ChlorobenzeneHCID 7964—
反応物Diphenyl sulfoxideHCID 13679—
反応物MagnesiumHCID 5462224—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物Triphenylsulfonium chlorideHCID 61343—

反応手順

Into 400 g of dichloromethane was dissolved 40 g (0.2 mole) of diphenyl sulfoxide, and the resulting solution was agitated under ice-cool. And then, 65 g (0.6 mole) of trimethyl silyl chloride was added dropwise at the temperature not exceeding 20° C., at which temperature the mixture was aged for 30 minutes. Thereafter, a Grignard agent prepared separately from 14.6 g (0.6 mole) of a metal magnesium, 67.5 g (0.6 mol) of chlorobenzene, and 168 g of tetrahydrofurane (THF) was added dropwise into it at the temperature not exceeding 20° C. After the reaction mixture was aged for one hour, it was added by 50 g of water at the temperature not exceeding 20° C. to terminate the reaction, and then further by 150 g of water, 10 g of 12-N hydrochloric acid, and 200 g of diethyl ether. A water layer was taken out by separation and washed by 100 g of diethyl ether to obtain an aqueous triphenyl sulfonium chloride solution. This was used in the subsequent reaction without isolation procedures further.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202677B2
出典データセットuspto-grants-2012_06
ORD IDord-71d2164e01384454a1547b8371ff9982
出典メモuspto-grants-2012_06