Imidazole → 1,1,1-Trifluoro-4-iodo-2-butanol

HRID 1243618Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1243618
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N1C=CN=C1.[I:25]I.[F:27][C:28]([F:35])([F:34])[CH:29]([OH:33])[CH2:30][CH2:31]O>ClCCl>[F:27][C:28]([F:35])([F:34])[CH:29]([OH:33])[CH2:30][CH2:31][I:25]

Komponenten

6

Versuchsvorschrift

A solution of triphenylphosphine (1.09 g, 4.16 mmol) in dichloromethane (14 mL) was treated with imidazole (0.283 g, 4.16 mmol) and iodine (1.06 g, 4.16 mmol), respectively, to give an orange suspension. A solution of 4,4,4-trifluoro-1,3-butanediol (0.500 g, 3.47 mmol) in dichloromethane (4 mL) was added to the suspension and stirred for 20 minutes. The solid was removed by filtration and the filtrate was concentrated under reduced pressure without heat to yield a black oil. The crude oil was purified by silica gel chromatography, eluting with 100% dichloromethane, to give the product as an oil (0.640 g, 72%).

Aufarbeitung

  1. customrespectively, to give an orange suspension
  2. customThe solid was removed by filtration
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. temperaturewithout heat
  5. customto yield a black oil
  6. customThe crude oil was purified by silica gel chromatography
  7. washeluting with 100% dichloromethane

Quellen und Nachweise

ORD-Eintrag
ord-b709147a52554af893f0701a50fc4f75
Quelldatensatz
uspto-grants-2006_10
Patentnummer
US07119109B2

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