تفاعل #3082

ord-426a0ebf081b4289a13701855d6e1618

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture was then refluxed for 1 hour
  2. 2
    أخرىThe organic phase was then removed
  3. 3
    غسيلwashed with 20 ml of water
  4. 4
    أخرىThe aqueous phase was then removed
  5. 5
    استخلاصextracted twice with 20 ml of diethylether
  6. 6
    تجفيفThe combined ether extracts were dried over magnesium sulfate
  7. 7
    أخرىAfter that, the solvent was evaporated under vacuum

الإجراء التجريبي

To a solution of 3.0 g (15.4 mmoles) of (-)-8-chloro-6-hydroxy-octanoic acid (-)-(VI) and 0.06 g (0.8 mmoles) of pyridine in 40 ml toluene, 4.1 g (34.4 mmoles) of thionyl chloride were added slowly. The mixture was then refluxed for 1 hour, cooled to room temperature and added to 60 ml of ice water. The organic phase was then removed, washed with 20 ml of water and stirred for 4 hours with 35 ml of 2N NaOH. The aqueous phase was then removed, adjusted to a pH of 1 with 3N HCl and extracted twice with 20 ml of diethylether. The combined ether extracts were dried over magnesium sulfate. After that, the solvent was evaporated under vacuum. (+)-6,8Dichloro-octanoic acid (+)-(VII) was obtained in a yield of 2.6 g (80% of the theoretical yield). [α]D20 =+30.5° (c=1; benzene).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05731448uspto-grants-1998_03