تفاعل #6913

ord-50a401181684469192a5170e3a2ba065

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىPrepared
  2. 2
    درجة الحرارةwarmed
  3. 3
    درجة الحرارةto reflux under N2
  4. 4
    درجة الحرارةat reflux
  5. 5
    درجة الحرارةAfter cooling
  6. 6
    أخرىthe reaction to rt
  7. 7
    أخرىThe volatiles were removed
  8. 8
    workup.ADDITIONfrexh methanol was added to the resulting residue
  9. 9
    أخرىAgain, the volatiles were removed
  10. 10
    غسيلwashed with saturated potassium carbonate (aqueous)
  11. 11
    تجفيفThe organic layer was dried over sodium sulfate
  12. 12
    أخرىthe volatiles were removed

الإجراء التجريبي

Prepared according to Procedure K. 2-iso-Propylsulfonylacetonitrile (0.50 g, 3.39 mmol) was dissolved in THF and warmed to reflux under N2. Borane dimethylsulfide (2M, 1.7 mL, 3.39 mmol) was added dropwise and the reaction was stirred for an additional 40 minutes at reflux. After cooling the reaction to rt, HCl (2 M in MeOH) was added to the reaction slowly due to gas evolution. The volatiles were removed and frexh methanol was added to the resulting residue. Again, the volatiles were removed and the resulting residue was taken up in CH2Cl2 (25 mL) and washed with saturated potassium carbonate (aqueous). The organic layer was dried over sodium sulfate and the volatiles were removed to afford the title compound. GC-MS m/z 152 (MH+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07084147B2uspto-grants-2006_08