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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2380002생성일: 2026년 10월 25일

Dimethyl Sulfoxide → 1,1,1-Tris(4-(2-bromotetrafluoroethoxy)phenyl)ethane

https://huagongshe.com/reaction/2380002

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물Potassium HydroxideHCID 14797—
반응물1,2-Dibromo-1,1,2,2-tetrafluoroethaneHCID 31301—
반응물1,1,1-Tris(4-hydroxyphenyl)ethaneHCID 93118—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물1,1,1-Tris(4-(2-bromotetrafluoroethoxy)phenyl)ethaneHCID 1895646512.2%

반응 조건

온도35 °C

반응 단계

A 1 liter 5-necked round bottom flask is fitted with a mechanical stirrer, a Dean Stark trap topped with a nitrogen padded reflux condenser, and a thermocouple attached to a temperature controller. A mixture of DMSO (450 ml), toluene (150 ml), and 1,1,1 -tris(4'-hydroxyphenyl)ethane (55.1 g, 0.18 mole) is added to the flask under nitrogen purge. After stirring for 15 minutes under a vigorous nitrogen purge, potassium hydroxide (85 percent pellets, 80.Og, 1.2 mole) is slowly added to the reaction flask. The mixture is then stirred at reflux for 48 hours with azeotropic removal of water. The resulting suspension is cooled to 35° C. in an ice bath and 1,2-dibromotetrafluoroethane (155 g, 0.60 mole) is added at a rate that maintains a temperature of 30°-35° C. When the addition is complete, the mixture is heated to 50° C. with continuous stirring for 3 hours. After filtration, the solvents are removed by heating under vacuum on a rotary evaporator. The brown residue is purified by column chromatography on neutral alumina using hexane as eluent to provide as product 1,1,1-tris(4'-[2"-bromotetrafluoroethoxy]phenyl)ethane (18.3 g, 0.022 mole, 12 percent yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05364917
출처 데이터셋uspto-grants-1994_11
ORD IDord-97024c76b442445cb5db420328934071
출처 메모uspto-grants-1994_11