تفاعل #7896

ord-b804c6c0279240b3a7262672a29b0e17

المذيبات

ظروف التفاعل

درجة الحرارة
35°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGstirred for 20 minutes
  2. 2
    درجة الحرارةunder cooling with ice so that its internal temperature would not
  3. 3
    أخرىexceed 20° C.
  4. 4
    workup.STIRRINGby stirring for 30 minutes
  5. 5
    غسيلAfter the reaction mixture was washed with 50 ml of t-butylmethyl ether
  6. 6
    workup.ADDITIONthe aqueous solution was adjusted to pH 3–4 by the addition of 1M hydrochloric acid
  7. 7
    استخلاصextracted with ethyl acetate
  8. 8
    غسيلThe organic layer was washed with water
  9. 9
    تجفيفwith a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate
  10. 10
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure

الإجراء التجريبي

3.0 g of 4-benyloxybutanol and 182 mg of TEMPO (2,2,6,6-tetramethyl-1-piperidinyloxy, radical) were dissolved in a mixture composed of 60 ml of acetonitrile and 60 ml of phosphate buffer (pH 6.7). To this reaction mixture were added 20 ml of an aqueous solution of sodium chlorite (NaClO2) (3.8 g) and 0.5 ml of a 5% aqueous solution of sodium hypochlorite (NaClO), followed by stirring at 35° C. for 5.5 hours. The reaction mixture was adjusted to pH 8.0 by the addition of a 2M aqueous solution of sodium hydroxide, and stirred for 20 minutes. Thereafter, 84 ml of an aqueous solution of sodium sulfate (5.1 g) was added thereto under cooling with ice so that its internal temperature would not exceed 20° C. , followed by stirring for 30 minutes. After the reaction mixture was washed with 50 ml of t-butylmethyl ether, the aqueous solution was adjusted to pH 3–4 by the addition of 1M hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with water and then with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 3.3 g (102% yield) of the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07087624B2uspto-grants-2006_08