(Diethylamino)sulfur trifluoride → 5-Bromo-1-(1-fluoropropyl)-2,3-dimethoxybenzene

HRID 638946Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 638946
[Br:1][C:2]1[CH:3]=[C:4]([O:14][CH3:15])[C:5]([O:12][CH3:13])=[C:6]([CH:8](O)[CH2:9][CH3:10])[CH:7]=1.CCN(S(F)(F)[F:22])CC>C(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]([O:14][CH3:15])[C:5]([O:12][CH3:13])=[C:6]([CH:8]([F:22])[CH2:9][CH3:10])[CH:7]=1

Komponenten

4

Edukt 2

HCID 123472(Diethylamino)sulfur trifluorideHCID 14470708HCID 14470708, Verbindung

Produkt 1

HCID 686856045-Bromo-1-(1-fluoropropyl)-2,3-dimethoxybenzeneAusbeute 80 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a stirred solution of 1-(5-bromo-2,3-dimethoxyphenyl)propan-1-ol (400 mg, 1.45 mmol) in DCM (10 mL) at −78° C. was added DAST (0.58 mL, 4.36 mmol) and stirred the reaction for 10 min at −78° C., then warmed to 0° C. for 2 h. The reaction was quenched with water and saturated aqueous NH4Cl (100 mL), extracted with EtOAc, dried over NasSO4 and concentrated in vacuo. The crude product was purified by flash column chromatography on silica gel using 30% EtOAc in hexanes as an eluent to furnish 5-bromo-1-(1-fluoropropyl)-2,3-dimethoxybenzene (80%).

Aufarbeitung

  1. customthe reaction for 10 min at −78° C.
  2. customThe reaction was quenched with water and saturated aqueous NH4Cl (100 mL)
  3. extractionextracted with EtOAc
  4. customdried over NasSO4
  5. concentrationconcentrated in vacuo
  6. customThe crude product was purified by flash column chromatography on silica gel using 30% EtOAc in hexanes as an eluent

Quellen und Nachweise

ORD-Eintrag
ord-6c80cc6a6fbe4320ae9c060d4bcdb4ec
Quelldatensatz
uspto-grants-2010_04
Patentnummer
US07691843B2

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