반응 #2314286

ord-0fbff6eecf894940af7bdd948d3e542c

반응 방정식

Cl
HCl
CC(C)=CCCC1=CCC(CCc2ccc(O)cc2)CC1
phenol
CC(C)=CCCC1=CCC(CCc2ccc(O)cc2)CC1
4-[2-(4-(4-Methyl-3-pentenyl)-3-cyclohexenyl)ethyl]phenol
Cc1ccc(S(=O)(=O)[O-])cc1
tosylate
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
CCCCCC1=CCC(COc2ccc(CCC3CC=C(CCC=C(C)C)CC3)cc2)CC1
4-[2-(4-(4-Methyl-3-pentenyl)-3-cyclohexenyl)ethyl]-1-(4-pentyl-3-cyclohexenyl)methoxybenzene

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타To a round-bottom flask equipped with a stirbar
  2. 2
    추출extracted with 1:1 hexanes
  3. 3
    세척The combined organic layers are washed with brine
  4. 4
    건조dried over potassium carbonate
  5. 5
    농축the solution is concentrated in vacuo
  6. 6
    여과Filtration through silica gel using 10% ethyl acetate in hexanes
  7. 7
    기타gives the pure product

실험 절차

To a round-bottom flask equipped with a stirbar is added phenol 2G (R=4-Methyl-3-pentenyl) (5 g), tosylate 1H (R=n-pentyl) (5.95 g), cesium carbonate (7.45 g), and anhydrous dimethylforrnamide (50 mL). The reaction mixture is stirred overnight. It is then poured into 50 mL dilute HCl, and extracted with 1:1 hexanes:ethyl acetate. The combined organic layers are washed with brine and dried over potassium carbonate, and the solution is concentrated in vacuo. Filtration through silica gel using 10% ethyl acetate in hexanes gives the pure product.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06413448B1uspto-grants-2002_07