Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4742생성일: 2026년 10월 23일
Sulfuric Acid → alpha,alpha-Bis-acetyloxy-4-[1-(acetyloxy)-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]toluene
https://huagongshe.com/ko/reaction/4742
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | 2-(p-Tolyl)hexafluoroisopropanol | HCID 74829 | — |
| 촉매 | chromium (VI) trioxide | HCID 10219390 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | alpha,alpha-Bis-acetyloxy-4-[1-(acetyloxy)-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]toluene | HCID 14076668 | — |
반응 단계
To a solution of 156 g (0.60 mole) of 4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]toluene in 675 ml of acetic anhydride is added 135 ml of concentrated sulfuric acid at 0°. To the solution stirred at 0° is added a soluton of 168 g (1.68 mole) of chromium trioxide in 750 ml of acetic anhydride dropwise over a two-hour period. After stirring is continued for an additional two hours, the resulting reaction mixture is poured into five liters of ice and is diluted with five liters of water to obtain an aqueous mixture which is allowed to stand for 18 hours. An oily solid with water above it is obtained. Water is decanted from the oily solid. The solid is dissolved in ether to obtain a solution which is washed with water and sodium bicarbonate solution, dried with anhydrous magnesium sulfate, filtered and evaporated at reduced pressure to give an oily solid. The solid is triturated with ether, filtered and recrystallized from chlorobutane to give 60 g of α,α -bis-acetyloxy-4-[1-(acetyloxy)-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]toluene, m.p. 93°-94.6°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04727180 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-444e854447fe4b53ac481a298adcab6e |
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| 출처 메모 | uspto-grants-1988_02 |
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