تفاعل #1377508

ord-6c851f8cd07446e08062180c114a0b64

معادلة التفاعل

CCOC(=O)C(C)(C)O
Ethyl 2-hydroxyisobutyrate
CCN(CC)S(F)(F)F
Diethylaminosulphur trifluoride
CCOC(=O)C(C)(C)F
ethyl 2-fluoro-isobutyrate
المردود 101.4%

الكواشف

لا شيء

ظروف التفاعل

درجة الحرارة
-70°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONAfter completion of the addition
  2. 2
    درجة الحرارةto warm to room temperature
  3. 3
    workup.WAITstood for 3 hours
  4. 4
    أخرىovernight
  5. 5
    workup.ADDITIONThe reaction was then carefully added to ice with vigorous stirring
  6. 6
    استخلاصextract of the aqueous layer
  7. 7
    غسيلThe total organic fraction was washed with brine
  8. 8
    تجفيفdried over magnesium sulphate
  9. 9
    workup.DISTILLATIONthe solvent carefully distilled

الإجراء التجريبي

Ethyl 2-hydroxyisobutyrate (12.43 g) was stirred in dry methylene chloride (65 ml) at -70° C. under nitrogen. Diethylaminosulphur trifluoride (30.32 g) in dry methylene chloride (5 ml) was added slowly, maintaining the temperature at -70° C. After completion of the addition, the mixture was stirred at -70° C. for 1 hour and was then allowed to warm to room temperature, stood for 3 hours and then overnight. The reaction was then carefully added to ice with vigorous stirring, and the resultant methylene chloride layer combined with a further methylene chloride extract of the aqueous layer. The total organic fraction was washed with brine, dried over magnesium sulphate and the solvent carefully distilled, to leave ethyl 2-fluoro-isobutyrate as a bronze liquid (12.8 g); 1H NMR analysis indicated that this material was >95% pure, and contained 2-3% of ethyl methacrylate. NMR (CDCl3, 270 MHz) δ 1.31(3H,t), 1.58(6H,d), 4.25(2H,q) ppm; 1H NMR (CDCl3, 254 MHz, 19F) δ -148.0 (1F, septet) ppm.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05750778uspto-grants-1998_05