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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1993609생성일: 2026년 10월 25일

Potassium Carbonate → 1-Bromo-3-fluoro-5-(1,1,2,2-tetrafluoroethoxy)benzene

https://huagongshe.com/reaction/1993609

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1,1,2,2-Tetrafluoroethyl iodideHCID 136180—
반응물3-Bromo-5-fluorophenolHCID 21904636—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물1-Bromo-3-fluoro-5-(1,1,2,2-tetrafluoroethoxy)benzeneHCID 23655105—

반응 조건

온도70 °C

반응 단계

To a solution of 3-bromo-5-fluorophenol (104 mmol crude) and iodo-1,1,2,2,-tetrafluoroethane (28.4 g, 125 mmol) in DMSO (80 mL) was added K2CO3 (57.0 g, 420 mmol). The reaction mixture was sealed in a thick walled glass pressure round bottom flask and heated at 70° C. for 18 h. The reaction mixture was allowed to cool to room temperature, diluted with water (500 mL) and extracted with ether (3×200 mL). The combined ether layers were washed with 1N NaOH (2×200 mL), water (2×200 mL) and brine (200 mL). The organic layer was dried over sodium sulfate, filtered and concentrated. The residue was dissolved in ether (150 mL) and filtered through a plug of activated basic alumina. The filtrate was concentrated to give 1-bromo-3-fluoro-5-(1,1,2,2-tetrafluoroethoxy)benzene as a pale yellow oil (27.2 g, 88% for two steps) which was used without further purification LCMS: 1.91 min, [M+1] No Ionizable peak (2 min gradient, MeOH/H2O 0.1% TFA); HPLC: 3.76 min (4 min gradient, MeOH/H2O 0.2% PPA) Purity 100%; NMR: 400 MHz 1H (CDCl3) 7.19 ppm, 2H, m; 6.92 ppm, 1H, d, J=8.35 Hz; 5.88 ppm, 1H, tt; J=52.95 Hz and J=2.64 Hz.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07652023B2
출처 데이터셋uspto-grants-2010_01
ORD IDord-294b58d031944970be2c0be95b168c46
출처 메모uspto-grants-2010_01