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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 84976생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/84976

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Triphenylsulfonium BromideHCID 11984010—
반응물(Adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonic acid triethylammonium saltHCID 131731910—
용매ChloroformHCID 6212—
생성물Triphenylsulfonium ((1-adamantyl)methoxycarbonyl)difluoromethanesulfonateHCID 4422473292%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846966B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d6bb2c220ef44b70a03283ff2acd87a6
출처 메모uspto-grants-2014_09