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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1033755생성일: 2026년 10월 27일

2,3,5-Triiodobenzoic acid → HCID 15232644, 화합물

https://huagongshe.com/reaction/1033755

반응식

참여 물질

역할이름HCID투입량
반응물2,3,5-Triiodobenzoic acidHCID 6948—
반응물TriethylamineHCID 8471—
반응물2-DimethylaminopyridineHCID 21885—
반응물Oxalyl chlorideHCID 65578—
반응물3,3,4,4,5,5,6,6,7,7,8,8-Dodecafluoro-2-octanolHCID 257710—
반응물2,3,5-Triiodobenzoyl chlorideHCID 2760806—
반응물2-Octyl-2,3,5-triiodobenzoateHCID 86747861—
용매DichloromethaneHCID 6344—
생성물HCID 15232644HCID 15232644—

반응 조건

온도0 °C

반응 단계

Using the same procedure as for 2-octyl-2,3,5-triiodobenzoate, 2,3,5-triiodobenzoyl chloride was prepared from 2.00 g of 2,3,5-triiodobenzoic acid and 2.54 g of oxalyl chloride in dry dichloromethane. The 2,3,5-triiodobenzoyl chloride was dissolved in 8 ml of dry dichloromethane. The solution was cooled to 0° C. and 0.810 g (8.00 mmol) of triethylamine was added. The brown solution was placed under nitrogen before 1.52 g (4.40 mmol) of 3,3,4,4,5,5,6,6,7,7,8,8-dodecafluoro-2-octanol was added dropwise. Dimethylaminopyridine (0.049 g, 0.400 mmol) was added and the resulting solution was stirred at room temperature for 18 hrs. The brown solution was then partitioned between 100 ml of dichloromethane and 50 ml of 1M HCl. The dichloromethane layer was washed with saturated NaHCO3 solution (50 ml) and brine (25 ml). The solution was dried over Na2SO4 and concentrated in vacuo to yield 3.11 g of a brown oil. The oil was purified by flash chromatography using 125 g of silica gel and 4% ethyl acetate/hexane as the eluent. The first 475 ml to elute contained nothing, while the pure product eluted with the next 200 ml. Concentration in vacuo afforded 2.36 g (71%) of the product as a colorless oil which slowly solidified to a white, waxy solid. Mp. 32°-35° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05312616
출처 데이터셋uspto-grants-1994_05
ORD IDord-fe73c769af2e46439029445b5af12981
출처 메모uspto-grants-1994_05