1,3-Dibromopropane → 7-Bromo-8-fluoro-3,4-dihydro-2H-benzo-[1,4]-dioxepine

HRID 1754061Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1754061
[Br:1][C:2]1[CH:3]=[C:4](O)[C:5]([OH:9])=[CH:6][C:7]=1[F:8].[C:11]([O-])([O-])=[O:12].[Cs+].[Cs+].BrC[CH2:19][CH2:20]Br>CN(C=O)C>[Br:1][C:2]1[C:7]([F:8])=[CH:6][C:5]2[O:9][CH2:20][CH2:19][O:12][CH2:11][C:4]=2[CH:3]=1

Komponenten

5

Edukt 3

HCID 80011,3-DibromopropaneHCID 10796Cesium carbonateHCID 218653784-Bromo-5-fluorobenzene-1,2-diol

Produkt 1

HCID 896220067-Bromo-8-fluoro-3,4-dihydro-2H-benzo-[1,4]-dioxepine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

To 1.50 g (7.25 mmol) of 4-bromo-5-fluorobenzene-1,2-diol in 25 ml DMF are added 5.90 g (18.1 mmol) Cs2CO3 and 0.89 ml (8.70 mmol) 1,3-dibromopropane. The reaction mixture is stirred at 120° C. over night. The solvent is removed in vacuo and to the residue is added water. After extracting with EtOAc the org. phases are combined, washed with sat. aq. NaCl solution and dried over MgSO4. The solvent is removed in vacuo and the resulting residue is purified by column chromatography (silica gel, PE/EtOAc 9/1→7/3).

Aufarbeitung

  1. customThe solvent is removed in vacuo and to the residue
  2. additionis added water
  3. extractionAfter extracting with EtOAc the org
  4. washwashed with sat. aq. NaCl solution
  5. dry with materialdried over MgSO4
  6. customThe solvent is removed in vacuo
  7. customthe resulting residue is purified by column chromatography (silica gel, PE/EtOAc 9/1→7/3)

Quellen und Nachweise

ORD-Eintrag
ord-f1748e75296d410dba083920eea77c53
Quelldatensatz
uspto-grants-2015_10
Patentnummer
US09169205B2

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