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Potassium tert-butoxide → HCID 86700852, Verbindung

HRID 881749
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 881749
[Cl-].[CH3:2][O:3][CH3:4].[C:5]1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CC(C)([O-])C.[K+].[Br:30][CH:31]1[C:36]2([C:39]3[CH:44]=[CH:43][C:42]([Cl:45])=[CH:41][CH:40]=3)[CH2:37][CH2:38][C:33](C=O)([CH2:34][O:35]2)[CH2:32]1>O1CCCC1>[Br:30][CH:31]1[C:36]2([C:39]3[CH:44]=[CH:43][C:42]([Cl:45])=[CH:41][CH:40]=3)[CH2:37][CH2:38][C:33]([CH:5]=[CH:2][O:3][CH3:4])([CH2:34][O:35]2)[CH2:32]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 23665647Potassium tert-butoxideHCID 86700850HCID 86700850, VerbindungHCID 86700853HCID 86700853, Verbindung

Produkt 1

HCID 86700852HCID 86700852, VerbindungAusbeute 95 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To a solution of triphenylphosphine methoxymethane chloride (3.51 g, 10.24 mmol) in tetrahydrofuran (20 ml) under nitrogen at room temperature, was added potassium t-butoxide (1.149 g, 10.24 mmol). The reddish solution was stirred at room temperature for 90 minutes. Then a solution of 6-bromo-1-(4-chloro-phenyl)-2-oxa-bicyclo[2.2.2]octane-4-carbaldehyde (2.25 g, 6.83 mmol) in tetrahydrofuran (6 ml) was added to the reaction mixture. The reaction mixture was stirred at room temperature for 10 minutes and then quenched with water (2 ml). The mixture was partitioned between brine (15 ml) and ethyl acetate (60 ml). The aqueous layer was extracted with ethyl acetate (2×30 ml) and the combined organic extracts were washed with brine, dried over Na2SO4, and concentrated. The residue was purified by flash chromatography (heptanes/acetone 2/1) to afford the cis and trans mixtures of 6-bromo-1-(4-chloro-phenyl)-4-(2-methoxy-vinyl)-2-oxa-bicyclo[2.2.2]octane (2.32 g, 95%) as colorless oil. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.74-2.99 (m, 6H) 3.54 (3.89 (m, 4H) 3.91-6.36 (m, 5H) 7.28-7.43 (m, 4H).

Aufarbeitung

  1. stirringThe reaction mixture was stirred at room temperature for 10 minutes
  2. customquenched with water (2 ml)
  3. customThe mixture was partitioned between brine (15 ml) and ethyl acetate (60 ml)
  4. extractionThe aqueous layer was extracted with ethyl acetate (2×30 ml)
  5. washthe combined organic extracts were washed with brine
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated
  8. customThe residue was purified by flash chromatography (heptanes/acetone 2/1)

Quellen und Nachweise

ORD-Eintrag
ord-42920343c21b4535bc1decb24c3dacf7
Quelldatensatz
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08993619B2

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