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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58518생성일: 2026년 10월 26일

Sodium Hydroxide → Triphenylsulfonium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenyl propionate

https://huagongshe.com/reaction/58518

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물1,4-DioxaneHCID 31275—
반응물Triphenylsulfonium chlorideHCID 61343—
반응물2-Ethoxycarbonyl-2,2-difluoro-1-phenylethyl 1-adamantanecarboxylateHCID 117966692—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물Triphenylsulfonium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenyl propionateHCID 13173701558%

반응 단계

After stirring a mixed solution of 1-adamantane carboxylic acid 2-ethoxycarbonyl-2,2-difluoro-1-phenyl-ethyl ester (6.6 g) prepared in Synthesis Example 1-5, 1,4-dioxane (20 g) and 25% by mass of caustic soda (2.5 g) for 2 hours, water (30 g) was added to the reaction solution and washed with n-hexane to prepare an aqueous solution of sodium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenyl propionate. An aqueous solution of triphenylsulfonium chloride (32 g) and methylene chloride (100 g) were added to the product, stirred for 30 minutes, and then an organic layer was isolated and washed with water, and thereafter was concentrated under reduced pressure. Methylisobutyl ketone was added to the concentrated solution, and concentrated again. Diisopropyl ether was added to the concentrated solution for crystallization, and a solid obtained was dried under reduced pressure to obtain a target compound, or triphenylsulfonium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenyl propionate (5.5 g) as a white crystal (yield: 58%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09436083B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-fe5ebfbe225e49188c545315d78d274f
출처 메모uspto-grants-2016_09