Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 428935Erstellt: 23. Oktober 2026

Nitric Acid → 2-Methyl-1-(3-nitrophenyl)-1-propanone

https://huagongshe.com/de/reaction/428935

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitric AcidHCID 944—
EduktIsobutyrophenoneHCID 69144—
EduktSulfuric acid, mixt. with nitric acidHCID 71777668—
LösungsmittelSulfuric AcidHCID 1118—
Produkt2-Methyl-1-(3-nitrophenyl)-1-propanoneHCID 14924012—

Reaktionsbedingungen

Temperatur-5 °C

Reaktionsschritte

Concentrated nitric acid (20 ml) was added cautiously with cooling to concentrated sulphuric acid (50 ml) maintaining a temperature of −5° C. Another solution of 2-methyl-1-phenyl-1-propanone (29.6 g, 0.2 mol) in concentrated sulphuric acid (70 ml) was made up with shaking, keeping the temperature at −5° C. The former nitric acid/sulphuric acid solution was added portionwise over 30 min to the latter solution of ketone in sulphuric acid keeping the temperature at −10° C.+/−5° C. during the addition and for a subsequent 30 min. The reaction mixture was poured onto crushed ice (1 l) and then extracted with diethyl ether (3×100 ml). The organic extracts were washed with water (300 ml) and then brine (300 ml), dried (Na2SO4) and then concentrated in vacuo. The crude product was obtained as an orange oil (40 g) which was purified by chromatography on silica gel (450 g) eluting with hexane :diethyl ether (9:1) to give the title compound as a pale yellow solid (16.3 g, 42%), m.p.33-35° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06313312B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-3eb7af1ac93044a6bb2b54e23dbca28a
Quellennotizuspto-grants-2001_11