Bromochloromethane → 2-Bromo-4-methoxy-8,9-dihydro-5,7-dioxabenzocycloheptene

HRID 2079214

Reaktionsgleichung

Reaktionsgleichung von HRID 2079214
[Br:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[C:5]([OH:10])=[C:4]([CH2:11][CH2:12][OH:13])[CH:3]=1.F[C:15](F)(F)C(O)=O.C(C1C=CC(NC(C2C=C(OC)C(OC)=CC=2F)C2NC(=O)N(C3C=CC=CC=3C(O)=O)N=2)=CC=1)(=N)N.C[Si]([N-][Si](C)(C)C)(C)C.[Na+].BrCCl.[Cl-].[NH4+]>CN(C=O)C.C(OCC)(=O)C>[Br:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[C:5]2[O:10][CH2:15][O:13][CH2:12][CH2:11][C:4]=2[CH:3]=1

Komponenten

8

Edukt 5

HCID 6333BromochloromethaneHCID 25517Ammonium ChlorideHCID 2724254Sodium bis(trimethylsilyl)amideHCID 670974744-Bromo-2-(2-hydroxyethyl)-6-methoxyphenolHCID 1363370832-{3-[(4-carbamimidoylphenylamino)-(2-fluoro-4,5-dimethoxyphenyl)methyl]5-oxo-4,5-dihydro-[1,2,4]triazol-1-yl}benzoic Acid Trifluoroacetate

Produkt 1

HCID 595172132-Bromo-4-methoxy-8,9-dihydro-5,7-dioxabenzocycloheptene

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6228DimethylformamideLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

To a solution of 898 mg of 4-bromo-2-(2-hydroxyethyl)-6-methoxyphenol in 10 ml of DMF there was added 1g of sodium bistrimethylsilylamide while cooling on ice, and the mixture was stirred at room temperature for 30 minutes. After adding 1 ml of bromochloromethane to the reaction mixture, it was stirred at 80° C. for 20 hours under a nitrogen atmosphere. Saturated aqueous ammonium chloride was added to the reaction mixture, and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (420 mg) as an oil.

Aufarbeitung

  1. temperaturewhile cooling on ice
  2. stirringwas stirred at 80° C. for 20 hours under a nitrogen atmosphere
  3. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  4. filtrationThe desiccating agent was filtered off
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (ethyl acetate-heptane)

Quellen und Nachweise

ORD-Eintrag
ord-6cdf322c9208499c9ad44f478544183f
Quelldatensatz
uspto-grants-2011_04
Patentnummer
US07928228B2

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