Reaktion #2068633

Reaktionsgleichung

(+)-2-Methylbutylbenzene

nitric acid

→

product

Ausbeute 38.0%

(+)-4-(2-methylbutyl)-nitrobenzene

Ausbeute 38.0%

Lösungsmittel

acetic acid

acetic acid

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONThis solution was added dropwise to a mixture of 420 ml 90%
2. 2
   TemperaturMaintaining that temperature
3. 3
   ExtraktionThe reaction products were extracted with 2-500 ml portions of petroleum ether (30°-60° C.)
4. 4
   Waschenthe combined extracts were successively washed with water (2-100 ml portions)
5. 5
   TrocknenThe extract was dried over anhydrous calcium sulfate
6. 6
   Sonstigethe solvent was removed under reduced pressure
7. 7
   SonstigeThe fraction boiling at 158°-160° C. (14 mm Hg) was collected

Vorschrift

(+)-2-Methylbutylbenzene, prepared according to the procedure of Example 2, (0.75 mol, 111.0 gm) was added to 200 ml glacial acetic acid. This solution was added dropwise to a mixture of 420 ml 90% fuming nitric acid and 180 ml glacial acetic acid, which had been cooled at -20° C. Maintaining that temperature, the mixture was stirred for one hour and then poured into 2.5 l of ice water. The reaction products were extracted with 2-500 ml portions of petroleum ether (30°-60° C.) and the combined extracts were successively washed with water (2-100 ml portions); 5% sodium hydroxide (2-100 ml portions), 10% sodium hydroxide (2-100 ml portions); and water (3-100 ml portions). The extract was dried over anhydrous calcium sulfate, the solvent was removed under reduced pressure and the resultant light yellow oil fractionated under reduced pressure. The fraction boiling at 158°-160° C. (14 mm Hg) was collected, giving a 38% yield of the product. The structure was confirmed by NMR.

Quelle