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HRID 647369作成日:2026年10月26日

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

https://huagongshe.com/reaction/647369

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物tert-ButanolHCID 6386—
反応物Potassium nitriteHCID 516910—
反応物1,1,1-Trifluoro-5-(2-methylphenyl)pentan-2-oneHCID 15568756—
溶媒WaterHCID 962—
生成物1,1,1-Trifluoro-3-(hydroxyimino)-5-(2-methylphenyl)pentan-2-oneHCID 7141414798%

反応条件

温度25 °C

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04408077
出典データセットuspto-grants-1983_10
ORD IDord-1fa0580bc644411981f725437587a388
出典メモuspto-grants-1983_10