تفاعل #814370

ord-67cdb9211e23479da5ad35178dce4616

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONUpon completion of addition
  2. 2
    workup.STIRRINGthe reaction mixture is stirred at ambient temperature for about one hour
  3. 3
    workup.ADDITIONUpon completion of addition
  4. 4
    درجة الحرارةto warm to ambient temperature where it
  5. 5
    workup.STIRRINGis stirred during about 18 hours
  6. 6
    تركيزAfter this time the reaction mixture is concentrated under reduced pressure to a residue
  7. 7
    workup.STIRRINGThe residue is stirred in water
  8. 8
    استخلاصthe mixture is extracted with three 50 mL portions of diethyl ether
  9. 9
    غسيلThe combined extracts are washed with water
  10. 10
    تجفيفdried with magnesium sulfate
  11. 11
    ترشيحThe mixture is filtered
  12. 12
    تركيزthe filtrate is concentrated under reduced pressure

الإجراء التجريبي

Under a nitrogen atmosphere, a mixture of 3.2 grams (0.08 mole) of sodium hydride (60% in mineral oil) in 25 mL of tetrahydrofuran is stirred, and a solution of 7.9 grams (0.08 mole) of trimethylsilylacetylene in 15 mL of tetrahydrofuran is added dropwise. Upon completion of addition, the reaction mixture is stirred at ambient temperature for about one hour. The reaction mixture is then cooled to 0° C., and a solution of 18.9 grams (0.08 mole) of 8-methylsulfonyloxy-1,4-dioxaspiro[4.5]decane in 25 mL of tetrahydrofuran is added dropwise. Upon completion of addition, the reaction mixture is allowed to warm to ambient temperature where it is stirred during about 18 hours. After this time the reaction mixture is concentrated under reduced pressure to a residue. The residue is stirred in water, and the mixture is extracted with three 50 mL portions of diethyl ether. The combined extracts are washed with water and dried with magnesium sulfate. The mixture is filtered, and the filtrate is concentrated under reduced pressure, yielding 8-trimethylsilylethynyl-1,4-dioxaspiro[4.5]decane.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05712281uspto-grants-1998_01