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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 84979생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/84979

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Triphenylsulfonium BromideHCID 11984010—
반응물(Adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonic acid tert-butylammonium saltHCID 131731911—
용매ChloroformHCID 6212—
생성물Triphenylsulfonium ((1-adamantyl)methoxycarbonyl)difluoromethanesulfonateHCID 4422473292%

반응 단계

Within a 1-L three-neck flask, 122 g (purity: 99%, 307 mmol, 1.0 eq) of the (adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonic acid tert-butylammonium salt obtained in Example 5-b was dissolved in 500 g of chloroform. To the resulting solution, 400 g of water and 110.5 g (322 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, 166 g of target triphenylsulfonium (adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonate was obtained (yield: 92%, purity: 99%). No fluorine ion (F−) was detected from any liquid waste of this step. Further, 200 ppb of sodium ion (Na+) was detected from the triphenylsulfonium (adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonate obtained in this step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846966B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-acfa2cd248d44fc8bd2cb4c3be34f306
출처 메모uspto-grants-2014_09