تفاعل #77958

ord-ebe185d583fa4cf3aed558a61bc0bef7

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصthe aqueous phase is extracted with ethyl acetate
  2. 2
    غسيلThe organic phase is washed with water
  3. 3
    تجفيفdried over magnesium sulfate
  4. 4
    تركيزconcentrated
  5. 5
    أخرىThe 2-methyl-6-nitrobenzonitrile can be purified by silica gel chromatography

الإجراء التجريبي

A solution of 16 g (150 mmol) of n-butyl nitrite (97% pure) and 7.7 g (50 mmol) of 3-nitro-o-xylene (97% pure) in 50 ml of dimethylformamide is cooled to from −5 to −10° C., and a solution of 11 g (100 mmol) of potassium tert-butoxide in 50 ml of dimethylformamide is added dropwise at this temperature, over a period of 1.5 hours. The reaction mixture is stirred at room temperature for another 6 days. For work-up, the mixture is poured into ice-water, the pH is adjusted to 1 using hydrochloric acid and the aqueous phase is extracted with ethyl acetate. The organic phase is washed with water, dried over magnesium sulfate and concentrated. This gives 8.2 g of product. The 2-methyl-6-nitrobenzonitrile can be purified by silica gel chromatography using toluene as mobile phase. M.p.: 101-103° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06706886B2uspto-grants-2004_03