Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1763062생성일: 2026년 10월 26일
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/1763062
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenol, 3-bromo-2,4,6-triiodo- | HCID 10218345 | — |
| 반응물 | 3,4-Dibromo-2,2,3,4,4-pentafluorobutanoyl chloride | HCID 14533537 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | (2,4,6-Triiodo-3-bromo-phenyl)-2,2,3,4,4-pentafluoro-3,4-dibromobutyrate | HCID 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=3080 (Ar-H); 1800 (C=O); 1550, 1520 (Ar C=C).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04835304 |
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| 출처 데이터셋 | uspto-grants-1989_05 |
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| ORD ID | ord-640341168d8647c49736b0879158ca91 |
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| 출처 메모 | uspto-grants-1989_05 |
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