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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41845생성일: 2026년 10월 24일

Sulfuric Acid → 1-Ethyl-4-trifluoromethylcyclohexanol

https://huagongshe.com/ko/reaction/41845

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Ethyl BromideHCID 6332—
반응물4-(Trifluoromethyl)cyclohexanoneHCID 2777491—
반응물MagnesiumHCID 5462224—
용매TetrahydrofuranHCID 8028—
생성물1-Ethyl-4-trifluoromethylcyclohexanolHCID 6475651170%

반응 조건

온도-5 °C

반응 단계

The inside of a reactor was sufficiently dried by vacuum heating, and the atmosphere inside the reactor was replaced with dry nitrogen. The reactor was charged with a Grignard reagent that was prepared in 350 ml of dehydrated tetrahydrofuran (dehydrated THF) using 9.7 g (0.40 mol) of a magnesium powder and 38.9 g (0.36 mol) of bromoethane 50 ml of a dehydrated THF solution of 49.8 g (0.30 mol) of 4-trifluoromethylcyclohexanone was added to the reactor over 15 minutes with stirring while cooling the solution at −5° C. using an ice bath. After increasing the temperature of the reactor to room temperature, the mixture was stirred for 2 hours. 500 ml of ice water and 100 ml of ice-cooled diluted sulfuric acid were then added to the mixture while sufficiently stirring the mixture. After separating the THF layer, the aqueous layer was extracted with diethyl ether to obtain an extract. The extract was combined with the THF layer, sequentially washed with a 5% sodium carbonate aqueous solution and water, and dried over sodium sulfate (desiccating agent). After removing sodium sulfate using a Buchner funnel, the organic solvent was evaporated. The residue was distilled under reduced pressure (30 mmHg). 1-Ethyl-4-trifluoromethylcyclohexanol was thus obtained (41.2 g (yield: 70%)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08535871B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-3eda108bfce74d3d871703601a0114d2
출처 메모uspto-grants-2013_09