(Diethylamino)sulfur trifluoride → 1-Bromo-3-(4-fluorobut-1-ynyl)benzene

HRID 30567Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 30567
[Br:1][C:2]1[CH:3]=[C:4]([C:8]#[C:9][CH2:10][CH2:11]O)[CH:5]=[CH:6][CH:7]=1.CCN(S(F)(F)[F:19])CC.C(=O)(O)[O-].[Na+]>C(Cl)Cl>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([C:8]#[C:9][CH2:10][CH2:11][F:19])[CH:3]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A solution of 1.5 gm (6.67 mmol) of 4-(3-bromophenyl)but-3-yn-1-ol in CH2Cl2 at 0° C. was treated with 2.0 mL (15.3 mmol) of DAST, stirred at 0° C. for 1 h, allowed to warm to room temperature for 1 h, poured into saturated sodium bicarbonate and extracted with EtOAc. The combined extracts were washed sequentially with water and brine, dried over Na2SO4 and concentrated under reduced pressure. Chromatography of the resultant concentrate on silica gel with a gradient of 0% to 24% EtOAc-hexanes gave 1-Bromo-3-(4-fluoro-but-1-ynyl)benzene as a volatile liquid, 0.96 gm (64% yield); 1H NMR (400 MHz, CDCl3) δ: 2.82 (dt, 2H, J=6.6, 19.8 Hz), 4.56 (dt, 2H, J=6.6,46.4 Hz), 7.14 (t, 2H, J=7.9 Hz), 7.31 (m, 1H), 7.41 (m, 1H), 7.55 (t, 1H, J=1.7 Hz).

Aufarbeitung

  1. temperatureto warm to room temperature for 1 h
  2. extractionextracted with EtOAc
  3. washThe combined extracts were washed sequentially with water and brine
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated under reduced pressure
  6. concentrationChromatography of the resultant concentrate on silica gel with a gradient of 0% to 24% EtOAc-hexanes

Quellen und Nachweise

ORD-Eintrag
ord-99ffb0a02dac4ab3ad52c77f7a062294
Quelldatensatz
uspto-grants-2008_09
Patentnummer
US07423158B2

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