5-Bromo-2-fluorobenzaldehyde → 4-Bromo-2-ethenyl-1-fluorobenzene

HRID 1241762Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1241762
[CH3:1]C(C)([O-])C.[K+].[Br:7][C:8]1[CH:9]=[CH:10][C:11]([F:16])=[C:12]([CH:15]=1)[CH:13]=O>[Br-].C[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C1COCC1>[Br:7][C:8]1[CH:9]=[CH:10][C:11]([F:16])=[C:12]([CH:15]=1)[CH:13]=[CH2:1]

Komponenten

5

Edukt 2

HCID 7363275-Bromo-2-fluorobenzaldehydeHCID 23665647Potassium tert-butoxide

Produkt 1

HCID 219339834-Bromo-2-ethenyl-1-fluorobenzeneAusbeute 90 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 74505Methyltriphenyliphosphonium bromideKatalysatorHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A mixture of methyltriphenylphosphonium bromide (2.14 g, 6 mmol) and potassium t-butoxide (672 mg, 6 mmol) in 50 mL of THF was refluxed for 30 minutes under N2 and then cooled to room temperature. 5-Bromo-2-fluorobenzaldehyde (1.02 g, 5 mmol) was added and the resulting mixture was refluxed for 2 hours (until the TLC showed the disappearance of starting aldehyde). The reaction was concentrated in vacuo and partitioned between water and ethyl acetate. The acetate layer was washed with water and brine. The solution was dried over MgSO4 and concentrated in vacuo. The residue was purified by chromatography (silica gel, 15:1 hexanes-diethyl ether) to provide 900 mg (90%) of 5-bromo-2-fluorostyrene.

Aufarbeitung

  1. temperaturewas refluxed for 30 minutes under N2
  2. temperaturethe resulting mixture was refluxed for 2 hours (until the TLC
  3. concentrationThe reaction was concentrated in vacuo
  4. custompartitioned between water and ethyl acetate
  5. washThe acetate layer was washed with water and brine
  6. dry with materialThe solution was dried over MgSO4
  7. concentrationconcentrated in vacuo
  8. customThe residue was purified by chromatography (silica gel, 15:1 hexanes-diethyl ether)

Quellen und Nachweise

ORD-Eintrag
ord-deec79f1804a4ca4a0de6e77ef4d3f82
Quelldatensatz
uspto-grants-2006_10
Patentnummer
US07115591B2

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