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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2372105생성일: 2026년 10월 27일

Iodine → 2-Chloro-1,1,1,4,4,4-hexafluorobutane

https://huagongshe.com/reaction/2372105

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참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물2,3-Dichloro-1,1,1,4,4,4-hexafluorobut-2-eneHCID 9337—
생성물2-Chloro-1,1,1,4,4,4-hexafluorobutaneHCID 273659641%

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온도250 °C

반응 단계

2,3-Dichlorohexafluorobut-2-ene (100 g) and iodine (55 g) were added to a 400 mL shaker tube. The tube was sealed, cooled, evacuated, and charged with 1500 psi of hydrogen at room temperature. The tube was then heated to 230° C. for 1 hour, 250° C. for 2 hours, and 260° C. for 15 hours. The tube was then cooled to room temperature, vented, and opened. The purple liquid was washed with water and then analyzed by GC/IR. Analysis of the washed liquid showed that it contained about 84% 2-chloro-1,1,1,4,4,4-hexafluorobutane, about 13% 2,3-dichloro-1,1,1,4,4,4-hexafluorobutane and about 1% 1,1,1,4,4,4-hexafluorobutane. The liquid was distilled on a concentric tube column yielding 35 g (41% isolated yield) of 2-chloro-1,1,1,4,4,4-hexafluorobutane (HCFC-346mdf) as a clear liquid with a b.p. of 50.9-51.4° C. 1H NMR (CHCl3 as internal standard): 4.4 ppm, complex, 1H; 2.9 ppm, complex, 1H; 2.7 ppm, complex, 1H. 19F NMR (CCl3F) as internal standard): 64.7 ppm, t, 1F; -76 ppm, d, 1F. GC/IR showed an identical spectrum to an authentic sample.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05097082
출처 데이터셋uspto-grants-1992_03
ORD IDord-3c7dfa0a7e954db78852163f254175c0
출처 메모uspto-grants-1992_03