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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 550328생성일: 2026년 10월 25일

Methane → 1,1,1-Trifluoro-2-trifluoromethyl-5-vinyloxy-pentan-2-ol

https://huagongshe.com/reaction/550328

반응식

참여 물질

역할이름HCID투입량
반응물MethaneHCID 297—
반응물Vinyl AcetateHCID 7904—
반응물Sodium CarbonateHCID 10340—
반응물5,5,5-Trifluoro-4-(trifluoromethyl)pentane-1,4-diolHCID 21895362—
촉매HCID 178478077HCID 178478077—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
생성물1,1,1-Trifluoro-2-trifluoromethyl-5-vinyloxy-pentan-2-olHCID 5876380225%

반응 조건

온도100 °C

반응 단계

1,1,1-Trifluoro-2-trifluoromethyl-2,5-pentanediol (11.3 g, 50 mmol), toluene (50 mL), sodium carbonate (10.6 g,100 mmol), chloro-1,5-cyclooctadiene iridium(I) dimer (0.34 g, 0.5 mmol), vinyl acetate(14 mL, 150 mmol) were placed in a dry 250 mL round-bottom flask equipped with a stir bar, condenser, and nitrogen inlet. The reaction mixture was heated to 100° C. and stirred for 3 hours, after which time it was cooled to room temperature. Diethyl ether (50 mL) was added to quench the reaction. After adding charcoal, the mixture was stirred for 1 hr and filtered with Celite 521. Diethyl ether, excess vinyl acetate, and solvent were distilled off under reduced pressure. The degree of the transetherification of the primary diol was found to be 52% by GC. Vacuum distillation (68-70° C., 15 mm Hg) afforded 3.13 g (25%) of colorless liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947425B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-916deb0365bf4401a69e629fbff88db9
출처 메모uspto-grants-2011_05