Nitric Acid → (+)-4-(2-Methylbutyl)-nitrobenzene

Temperature

-20 °C

(+)-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.

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

ORD record

ord-fc32edf66f844c31ac544ba8b2f622bb

Source dataset

uspto-grants-1983_07

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04394070