تفاعل #487504

ord-9569a0fca728472ab89020adcb2b87f5

معادلة التفاعل

CC(C)O
isopropyl alcohol
CC(C)O
isopropyl alcohol
CC(=O)OCC#CCCCCO[Si](C)(C)C(C)(C)C
( 28 )
CC(=O)OCC#CCCCCO[Si](C)(C)C(C)(C)C
Acetic acid 7-(tert-butyl-dimethyl-silanyloxy)-hept-2-ynyl ester
CC(C)=O.O=S(=O)(O)O.[O]=[Cr](=[O])=[O]
Jones Reagent
CC(=O)OCC#CCCCC(=O)O
oil
CC(=O)OCC#CCCCC(=O)O
7-Acetoxy-hept-5-ynoic acid

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةcooled with an ice bath
  2. 2
    workup.ADDITIONwas added
  3. 3
    workup.WAITAfter another 15 minutes
  4. 4
    ترشيحwas filtered through celite
  5. 5
    أخرىthe filtrate evaporated in vacuo
  6. 6
    أخرىThe residue was partitioned between 100 mL ether and 100 mL saturated ammonium chloride solution
  7. 7
    استخلاصThe aqueous layer was extracted with 100 mL ether
  8. 8
    غسيلthe combined ether solution washed with brine
  9. 9
    تجفيفdried (MgSO4)
  10. 10
    ترشيحfiltered
  11. 11
    أخرىevaporated

الإجراء التجريبي

A solution of crude (28) in acetone (100 mL) was treated with Jones Reagent (18.0 mL, 41.4 mmol, 2.3 M) and cooled with an ice bath. After 1 hour at room temperature, 10 mL isopropyl alcohol was added and the mixture stirred for 15 minutes. The mixture still had a brown color so another 10 mL isopropyl alcohol was added. After another 15 minutes, the color had not changed so the mixture was filtered through celite and the filtrate evaporated in vacuo. The residue was partitioned between 100 mL ether and 100 mL saturated ammonium chloride solution. The aqueous layer was extracted with 100 mL ether and the combined ether solution washed with brine and then dried (MgSO4), filtered and evaporated to leave a yellow oil (6.333 g) that was used directly in the next step.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08741281B2uspto-grants-2014_06