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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 647369Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/647369

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukttert-ButanolHCID 6386—
EduktPotassium nitriteHCID 516910—
Edukt1,1,1-Trifluoro-5-(2-methylphenyl)pentan-2-oneHCID 15568756—
LösungsmittelWaterHCID 962—
Produkt1,1,1-Trifluoro-3-(hydroxyimino)-5-(2-methylphenyl)pentan-2-oneHCID 7141414798%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

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%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04408077
Quelldatensatzuspto-grants-1983_10
ORD IDord-1fa0580bc644411981f725437587a388
Quellennotizuspto-grants-1983_10