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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 647369생성일: 2026년 10월 26일

Acetic Acid → 1,1,1-Trifluoro-3-(hydroxyimino)-5-(2-methylphenyl)pentan-2-one

https://huagongshe.com/reaction/647369

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물tert-ButanolHCID 6386—
반응물Potassium nitriteHCID 516910—
반응물1,1,1-Trifluoro-5-(2-methylphenyl)pentan-2-oneHCID 15568756—
용매WaterHCID 962—
생성물1,1,1-Trifluoro-3-(hydroxyimino)-5-(2-methylphenyl)pentan-2-oneHCID 7141414798%

반응 조건

온도25 °C

반응 단계

A solution of potassium nitrite (22.2 g, 0.26 mol) in water (total volume=7.4 mL) was added in one portion to a stirred solution of 1,1,1-trifluoro-5-(2-methylphenyl)-2-pentanone (20 g, 0.087 mol), tert-butanol (25 mL) and acetic acid (25 mL) at 25° C. The reaction mixture was stirred at 25° C. for 2.5 hr. Another solution of potassium nitrite (7.5 g, 0.088 mol) in water (2.5 mL) then was added. After stirring for 1.5 hr, the reaction mixture was poured into water. The resulting mixtutre was extracted with diethyl ether (3x). The combined ether extracts were washed with water and then washed with a saturated aqueous solution of NaHCO3. Thereafter, the organic extract was dried (MgSO4) and concentrated under reduced pressure to give the title compound (22.1 g, 98% yield) as a yellow crystalline mass. This product was used for the reaction described in the following example. A sample of the product, recrystallized for hexane, had mp 80°-81° C.; nmr (CDCl3) δ 2.35 (s, 3H), 2.8 (s, 4H), 7.1 (s, 4H); ir (CHCl3) 3540, 3340, 1730, 1165-1 ; Anal Calcd for C12H12F3NO2 : C, 55.60% H, 4.67%; Found: C, 55.41% H, 4.60%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04408077
출처 데이터셋uspto-grants-1983_10
ORD IDord-1fa0580bc644411981f725437587a388
출처 메모uspto-grants-1983_10