تفاعل #77953

ord-5ea4bc75f9f648a18d19f8443d30ff76

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصthe aqueous phase is extracted with methylene chloride
  2. 2
    غسيلThe organic phase is washed with sodium bicarbonate solution
  3. 3
    تجفيفdried over magnesium sulfate
  4. 4
    تركيزconcentrated
  5. 5
    أخرىThis gives 18.4 g of a light-beige crude product which is purified by recrystallization from approximately 30 ml of toluene

الإجراء التجريبي

A solution of 12.7 g (119 mmol) of n-butyl nitrite (97% pure) and 20 g (92 mmol) of 2,3-dimethyl-4-methylsulfonylchlorobenzene in 100 ml of dimethylformamide is cooled to from −55 to −60° C., and a solution of 16.8 g (147 mmol) of potassium tert-butoxide in 70 ml of dimethylformamide is added dropwise at this temperature, over a period of 30 minutes. The reaction is monitored by HPLC. For work-up, initially 50 ml of water are added, and the pH is subsequently adjusted to 5-6 using approximately 30 ml of glacial acetic acid. The reaction mixture is subsequently poured into 0.7 kg of ice-water, and the aqueous phase is extracted with methylene chloride. The organic phase is washed with sodium bicarbonate solution, dried over magnesium sulfate and concentrated. This gives 18.4 g of a light-beige crude product which is purified by recrystallization from approximately 30 ml of toluene.

المصدر

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