تفاعل #66061

ord-788482f2c86d4fcf85ad7c5a22fe736c

معادلة التفاعل

CO
Methanol
O=C1CN2CCC1CC2
quinuclidin-3-one
CCCCCC.C[Si](C)(C)C=[N+]=[N-]
(trimethylsilyl)diazomethane hexane
O=C1CCN2CCC1CC2
titled compound
O=C1CCN2CCC1CC2
1-azabicyclo[3.2.2]nonan-4-one

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىquenched
  2. 2
    workup.ADDITIONto colorless by addition of acetic acid
  3. 3
    workup.WAITAfter a few minutes
  4. 4
    workup.ADDITIONsaturated aqueous sodium carbonate (15 mL) was added
  5. 5
    أخرىThe organic layer was separated
  6. 6
    استخلاصthe aqueous solution was extracted with methylene chloride (3×50 mL)
  7. 7
    تجفيفThe combined organic layer and extracts were dried over magnesium sulfate
  8. 8
    تركيزconcentrated in vacuo

الإجراء التجريبي

An ice-cooled solution (5° C.) of (trimethylsilyl)diazomethane/hexane (2 N, 30 mL, 60 mmol; Aldrich) under nitrogen was treated dropwise with a solution of quinuclidin-3-one (7500 mg, 60 mmol) in dry tetrahydrofuran (40 mL). Methanol (20 mL) was added, and the yellow solution was warmed to room temperature, stirred for 24 hours, and quenched to colorless by addition of acetic acid. After a few minutes, saturated aqueous sodium carbonate (15 mL) was added. The organic layer was separated, and the aqueous solution was extracted with methylene chloride (3×50 mL). The combined organic layer and extracts were dried over magnesium sulfate, and concentrated in vacuo to give the titled compound. The material was used directly for next step without further purification.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08524703B2uspto-grants-2013_09