تفاعل #927237

ord-93449926e59843698ca9d007784759f4

معادلة التفاعل

[H-].[Na+]
sodium hydride
NC(=O)C(F)(F)F
trifluoroacetamide
C#CCCCCCCI
8-iodo-1-octyne
[Cl-].[NH4+]
ammonium chloride
C#CCCCCCCNC(=O)C(F)(F)F
8-trifluoroacetamido-1-octyne
المردود 79.5%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added portionwise with ice cooling
  2. 2
    تجفيفThe ether layer was dried over magnesium sulfate
  3. 3
    تركيزconcentrated under reduced pressure
  4. 4
    أخرىthe resulting residue was purified by silica gel column chromatography (eluent; hexane-ethyl acetate mixed solvent)
  5. 5
    أخرىcrystallized from hexane

الإجراء التجريبي

To a solution of sodium hydride (60% oil, 9.82 g, 245 mmol) in DMF (200 ml), trifluoroacetamide (34.7 g, 307 mmol) divided into 10 portion was added portionwise with ice cooling. Then, the reaction mixture was added with a solution of 8-iodo-1-octyne (14.5 g, 61.4 mmol) in DMF (60 ml), and stirred at room temperature for two hours. The reaction mixture was added with saturated aqueous ammonium chloride (400 ml) and ether (400 ml) for extraction. The ether layer was dried over magnesium sulfate, and concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (eluent; hexane-ethyl acetate mixed solvent), and crystallized from hexane to afford 10.8 g of 8-trifluoroacetamido-1-octyne (yield; 79.3%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06365350B1uspto-grants-2002_04