反応 #487504

ord-9569a0fca728472ab89020adcb2b87f5

反応方程式

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

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度cooled with an ice bath
  2. 2
    workup.ADDITIONwas added
  3. 3
    workup.WAITAfter another 15 minutes
  4. 4
    ろ過was filtered through celite
  5. 5
    その他the filtrate evaporated in vacuo
  6. 6
    その他The residue was partitioned between 100 mL ether and 100 mL saturated ammonium chloride solution
  7. 7
    抽出The aqueous layer was extracted with 100 mL ether
  8. 8
    洗浄the combined ether solution washed with brine
  9. 9
    乾燥dried (MgSO4)
  10. 10
    ろ過filtered
  11. 11
    その他evaporated

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08741281B2uspto-grants-2014_06