Tetrabutylammonium Fluoride → 4-[1,3]Dioxolan-2-yl-2-fluorophenol

HRID 228437Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 228437
[O:1]1[CH2:5][CH2:4][O:3][CH:2]1[C:6]1[CH:22]=[CH:21][C:9]([O:10][Si](C(C)C)(C(C)C)C(C)C)=[C:8]([F:23])[CH:7]=1.[F-].C([N+](CCCC)(CCCC)CCCC)CCC.CCCCCCC.C(OCC)(=O)C>C1COCC1.ClCCl>[O:1]1[CH2:5][CH2:4][O:3][CH:2]1[C:6]1[CH:22]=[CH:21][C:9]([OH:10])=[C:8]([F:23])[CH:7]=1

Komponenten

6

Edukt 3

HCID 2724141Tetrabutylammonium FluorideHCID 21899848Ethylacetate heptaneHCID 59730094(4-[1,3]Dioxolan-2-yl-2-fluorophenoxy)triisopropylsilane

Produkt 1

HCID 184436734-[1,3]Dioxolan-2-yl-2-fluorophenolAusbeute 52 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6344DichloromethaneLösungsmittelHCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To a solution of (4-[1,3]dioxolan-2-yl-2-fluorophenoxy)triisopropylsilane (Example 93. Part B) (105.9 g, approximately 0.311 mol) in THF (1.589 L) add 1.0 M tetrabutylammonium fluoride (TBAF) in THF (311 mL) in a steady stream over 5 min at 23-27° C. without cooling. Stir for 1 hr till the reaction complete by TLC (19:1 heptane/ethyl acetate). Concentrate to a red oil and partition between ether (500 mL) and deionized water (1 L). Separate the layers and extract the aqueous layer with ether (500 mL). Combine the ether layers, wash with brine and dry over sodium sulfate. Filter and concentrate to give the crude product (92.9 g. Dissolve the crude product in dichloromethane and filter through 400 g of silica gel 60. Wash with dichloromethane (3×1 L fractions) and concentrate the combined filtrate to give an impure product. Crystallize from dichloromethane/heptane to give the title compound (29.8 g, 52%). Gas chromatography: retention time 15.96 min (30 m×0.32 mm i.d. DB-1 column, 0.25 micron film thickness; 1.2 mL/min flow rate; 55:1 split ratio; temperature profile: 35° C./3 min, 10° C. temperature increase per min; 250° C./10.5 min). 1H NMR (DMSO-d6) δ 3.84-3.93 (m, 2H, CH2), 3.93-4.04 (m, 2H, CH2), 5.60 (s, 1H, CH), 6.91 (t, 11, ArH), 7.06 (dd, 1H, ArH), 7.15 (dd, 1H, ArH), 10.0 (s, 1H, OH).

Aufarbeitung

  1. temperaturewithout cooling
  2. concentrationConcentrate to a red oil
  3. custompartition between ether (500 mL) and deionized water (1 L)
  4. customSeparate the layers
  5. extractionextract the aqueous layer with ether (500 mL)
  6. washCombine the ether layers, wash with brine
  7. dry with materialdry over sodium sulfate
  8. filtrationFilter
  9. concentrationconcentrate
  10. customto give the crude product (92.9 g
  11. filtrationfilter through 400 g of silica gel 60
  12. washWash with dichloromethane (3×1 L fractions)
  13. concentrationconcentrate the combined filtrate
  14. customto give an impure product
  15. customCrystallize from dichloromethane/heptane

Quellen und Nachweise

ORD-Eintrag
ord-4ff33d8afeec4c988535f2e0fc84f082
Quelldatensatz
uspto-grants-2009_07
Patentnummer
US07560463B2

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