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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6312생성일: 2026년 10월 25일

Phenol, 3-bromo-2,4,6-triiodo- → (2,4,6-Triiodo-3-bromo-phenyl)-2,2,3,4,4-pentafluoro-3,4-dibromobutyrate

https://huagongshe.com/reaction/6312

반응식

참여 물질

역할이름HCID투입량
반응물Phenol, 3-bromo-2,4,6-triiodo-HCID 10218345—
반응물3,4-Dibromo-2,2,3,4,4-pentafluorobutanoyl chlorideHCID 14533537—
용매PyridineHCID 1049—
생성물(2,4,6-Triiodo-3-bromo-phenyl)-2,2,3,4,4-pentafluoro-3,4-dibromobutyrateHCID 14533542—

반응 단계

20.3 grams of 3-bromo-2,4,6-triiodophenol (m.p 155°-157° C.) were dissolved in 50 ml of pyridine 13.0 grams of 2,2,3,4,4-pentafluoro-3,4-dibromo-butyryl chloride were added dropwise through a dropping funnel with stirring. The mixture was stirred overnight at room temperature. The mixture was washed in a separatory funnel twice with 250 ml of DI water, then filtered through a column of silica and the solvent evaporated. The material was then chromatographed on a column of silica using FREON 113 (trichlorotrifluroethane) as eluent. The sample (25 grams), which slowly crystallized at room temperature, was shown to be pure ester (97%) by gc/ms. It is suitable for use as a fluid above its melting point of 56°-57° C. m/e (chemical ionization) 129 (21%, CF2Br); 131 (100%, CF2Br and C3F5); 140 (13%, C5HBr); 142 (13%, C5HBr); 188 (14%, C5HI); 267, 269 (11%, 10% C5BrIH); 315 (4%, C5I2H); 422, 424 (6%, 7%, C6I2HBrO); 549, 551 (5%, 4%, C6I3HBrO); 866, 868, 870, 872 (0.2%, 0.6%, 0.4%, 0.2%, molecular ion). I.R.(ν, in cm-1) =3080 (Ar--H); 1800 (C=O); 1550, 1520 (Ar C=C).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05248432
출처 데이터셋uspto-grants-1993_09
ORD IDord-af04e3fc60fd4e9a9acc5f15ce50eda6
출처 메모uspto-grants-1993_09