تفاعل #5365

ord-6ebe688ebcaa44038748c3ce2deef2cf

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىas described in the preparation of Example 52
  2. 2
    workup.ADDITIONTo this mixture is added 1.50 g of Aliquot 336
  3. 3
    أخرىseparated from the organic phase
  4. 4
    استخلاصextracted three times with dichloromethane
  5. 5
    غسيلThe combined organic layers are washed with water
  6. 6
    تجفيفdried over MgSO4
  7. 7
    تركيزconcentrated in vacuo

الإجراء التجريبي

Cis-nonen-1-ol (10.0 g) is subjected to the cyclopropanation conditions as described in the preparation of Example 52. The resulting residue is taken up in 100 mL of dichloromethane at 0° C., followed by the addition of 800 mg of sodium bromide in 2 mL of water and 150 mg of 2,2,6,6-tetramethyl-1-piperidinyloxy, free radical. To this mixture is added 1.50 g of Aliquot 336 followed by the dropwise addition of 9.2 g of sodium bicarbonate in 230 mL of 5% NaOCl. The aqueous phase is made basic, separated from the organic phase and acidified with concentrated HCl, and then extracted three times with dichloromethane. The combined organic layers are washed with water, dried over MgSO4, and concentrated in vacuo to give cis-2-(2'-pentylcyclopropyl)acetic acid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05242945uspto-grants-1993_09