Cyclopentadiene → 5-Fluoro-1,4-dihydro-1,4-methano-naphthalene

HRID 2180078Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2180078
F[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1I.[CH:10]1[CH2:14][CH:13]=[CH:12][CH:11]=1.[Li]CCCC>CCOCC>[F:8][C:4]1[CH:5]=[CH:6][CH:7]=[C:2]2[C:3]=1[CH:14]1[CH2:13][CH:12]2[CH:11]=[CH:10]1

Komponenten

5

Edukt 3

HCID 7612CyclopentadieneHCID 27827381,3-Difluoro-2-iodobenzeneHCID 178418339Butyllithium

Produkt 1

HCID 1437965-Fluoro-1,4-dihydro-1,4-methano-naphthalene

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

A solution of 2,6-difluoroiodobenzene (5.0 g, 20.8 mmol) and cyclopentadiene (2.07 g, 31.3 mmol) was stirred at 0° C. in P. ether (70 mL, 40-60° C.) under N2 and treated with n-BuLi (8.74 mL, 2.5M in hexanes, 21.8 mmol) dropwise over 10 minutes. The reaction was quenched after 15 minutes by addition of aqueous 1N HCl solution and the product was extracted with hexanes (3×50 mL). The combined organic layer was washed with H2O (50 mL), saturated aqueous NaCl solution (50 mL), dried (MgSO4), filtered and evaporated. Chromatography on Silica gel provided product as an oil (1.5 g, 45%) (TLC hexanes Rf 0.55). 1H NMR (400 MHz, CDCl3) δ 7.08 (ddd, J=7.0,1.0,0.8 Hz, 1H), 6.96 (ddd, J=8.5,8.3,7.0 Hz, 1H), 6.86 (br s, 2H), 6.72 (ddd, J=8.5,8.3,0.8 Hz, 1H), 4.25 (br s, 1H). 3.98 (br s, 1H), 2.36 (ddd, J=7.2,1.7,1.7 Hz, 1H), 2.30 (ddd, J=7.2,1.7,1.5 Hz, 1H). GCMS m/e 160 (M+).

Aufarbeitung

  1. customThe reaction was quenched after 15 minutes by addition of aqueous 1N HCl solution
  2. extractionthe product was extracted with hexanes (3×50 mL)
  3. washThe combined organic layer was washed with H2O (50 mL), saturated aqueous NaCl solution (50 mL)
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-3153cb541a24444fa6acb8ec530c69ff
Quelldatensatz
uspto-grants-2005_05
Patentnummer
US06887884B2

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