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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 723055생성일: 2026년 10월 26일

Hydrochloric Acid → 3'-Bromo-2,2,2-trifluoroacetophenone

https://huagongshe.com/reaction/723055

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl AcetateHCID 8857—
반응물Methyl 3-bromobenzoateHCID 12070—
반응물(Trifluoromethyl)trimethylsilaneHCID 552549—
촉매Tetrabutylammonium FluorideHCID 2724141—
용매TolueneHCID 1140—
생성물3'-Bromo-2,2,2-trifluoroacetophenoneHCID 1464744265%

반응 조건

온도-78 °C

반응 단계

In a dry round bottom flask, 3-bromo-benzoic acid methyl ester (2 g, 9.3 mmol, Aldrich Chemical Company) and trimethyl(trifluoromethyl)silane (1.72 mL, 11.6 mmol, Aldrich Chemical Company) were dissolved in dry toluene (50 mL). Upon cooling the solution to −78° C., TBAF (232 μL, 0.23 mmol) was added and the reaction was allowed to warm up slowly to rt overnight. After stirring for 20 hr, 2N HCl (50 mL) and EtOAc (100 mL) were added, the layers were separated, and the aqueous layer was extracted with another portion of EtOAc. The combined organic fractions were dried (MgSO4), concentrated in vacuo, and resulting crude oil was purified using SiO2 flash chromatography (elution: 5–20% EtOAc in hexanes) to give 1.5 g (65%) the title compound as a light yellow oil. 1H-NMR (CDCl3; 400 MHz) δ 8.18 (br s, 1H), 7.98–8.00 (m, 1H), 7.82–7.85 (m, 1H), 7.42–7.46 (m, 1H). 19F-NMR (CDCl3; 400 MHz) δ −72.06 (s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07138530B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-2b2cda64ac6944fca39ba598ad06d0d8
출처 메모uspto-grants-2006_11