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HRID 84976作成日:2026年10月25日

Water → Triphenylsulfonium ((1-adamantyl)methoxycarbonyl)difluoromethanesulfonate

https://huagongshe.com/reaction/84976

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Triphenylsulfonium BromideHCID 11984010—
反応物(Adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonic acid triethylammonium saltHCID 131731910—
溶媒ChloroformHCID 6212—
生成物Triphenylsulfonium ((1-adamantyl)methoxycarbonyl)difluoromethanesulfonateHCID 4422473292%

反応手順

Within a 1-L three-neck flask, 100 g (purity: 93%, 219 mmol, 1.0 eq) of the (adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonic acid triethylammonium salt obtained in Example 1-c was dissolved in 300 g of chloroform. To the resulting solution, 250 g of water and 78.9 g (223 mmol, 1.05 eq) of triphenylsulfonium bromide were added. This reaction solution was stirred for 1 hour. After the reaction, the reaction solution was separated into an organic layer and an aqueous layer. The organic layer was washed with water, followed by distillating chloroform from the washed organic layer. The thus-obtained concentrated solution was dissolved in a mixed solvent of chloroform, ethyl acetate and diisopropyl ether and then recrystallized. With this, 119 g of target triphenylsulfonium (adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonate was obtained (yield: 92%, purity: 99%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846966B2
出典データセットuspto-grants-2014_09
ORD IDord-d6bb2c220ef44b70a03283ff2acd87a6
出典メモuspto-grants-2014_09