تفاعل #66730

ord-5ce4ea56a24644e28963542948ca5db0

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe mixture was put into a preheated bath at 90° C
  2. 2
    درجة الحرارةThe mixture was heated until gas evolution
  3. 3
    أخرى(ca. 1.5 h)
  4. 4
    أخرىwas continued at 100° C
  5. 5
    درجة الحرارةit was cooled to room temperature
  6. 6
    استخلاصthe mixture was extracted twice with 1M aqueous sodium carbonate solution
  7. 7
    استخلاصThe aqueous layer was extracted with ethyl acetate
  8. 8
    تجفيفthe combined organic layer was dried over sodium sulphate
  9. 9
    أخرىevaporated

الإجراء التجريبي

0.7 g of 4-Oxo-adamantane-1-carboxylic acid (11) were codistilled twice with toluene and dissolved in 5.5 mL of dry toluene. 1.1 mL of triethylamine were added. At 0° C., 0.9 mL of diphenylphosphoryl azide were added dropwise. The mixture was allowed to warm to room temperature and then the mixture was put into a preheated bath at 90° C. The mixture was heated until gas evolution ceased (ca. 1.5 h). 1.9 mL of benzyl alcohol were added and stirring was continued at 100° C. When the reaction was complete, it was cooled to room temperature, then ethyl acetate was added and the mixture was extracted twice with 1M aqueous sodium carbonate solution. The aqueous layer was extracted with ethyl acetate and the combined organic layer was dried over sodium sulphate and evaporated. The resulting oil was subjected to silica gel chromatography (heptanes:ethyl acetate) to give 871 mg of the desired product. Rt=1.40 min (Method 3). Detected mass: 300.2 (M+H+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08524737B2uspto-grants-2013_09