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7-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-one → 7-fluoro-3,4-dihydro-2H-1,4-benzoxazine

HRID 901831
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 901831
O=[C:2]1[CH2:7][O:6][C:5]2[CH:8]=[C:9]([F:12])[CH:10]=[CH:11][C:4]=2[NH:3]1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[F:12][C:9]1[CH:10]=[CH:11][C:4]2[NH:3][CH2:2][CH2:7][O:6][C:5]=2[CH:8]=1
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Komponenten

4

Edukt 2

HCID 137312957-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-oneHCID 21226445Aluminium lithium hydride

Produkt 1

HCID 144229537-fluoro-3,4-dihydro-2H-1,4-benzoxazineAusbeute 65 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

3-Oxo-7-fluoro-3,4-dihydro-2H-benzo[b][1,4]oxazine (2.2 g, 1 eq, 13.1 mmol) obtained in step (ii) in dry THF (10 ml) was added drop wise to a refluxing THF (60 ml) containing LAH (1.5 g, 3 eq, 39.5 mmol). It was further refluxed for 3 h and quenched with ethyl acetate. To this water (1.5 ml), 15% sodium hydroxide (1.5 ml) and water (4.5 ml) were added sequentially. Once Al(OH)3.H2O precipitated out, it was filtered though celite. The filtrate was condensed on rotavapour and chromatographed (ethyl acetate and hexane) to yield 7-fluoro-3,4-dihydro-2H-benzo[b][1,4]oxazine (1.3 g, yield 65%) as yellow oil.

Aufarbeitung

  1. temperatureIt was further refluxed for 3 h
  2. customquenched with ethyl acetate
  3. additionTo this water (1.5 ml), 15% sodium hydroxide (1.5 ml) and water (4.5 ml) were added sequentially
  4. customOnce Al(OH)3.H2O precipitated out
  5. filtrationit was filtered though celite
  6. customcondensed on rotavapour
  7. customchromatographed (ethyl acetate and hexane)

Quellen und Nachweise

ORD-Eintrag
ord-f7458281483443b192f3d1980b42c05e
Quelldatensatz
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07365064B2

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