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

HRID 1243618Notes

Reaction equation

HRID 1243618 reaction equation
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]

Participants

6

Procedure

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%).

Workup

  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

Sources & evidence

ORD record
ord-b709147a52554af893f0701a50fc4f75
Source dataset
uspto-grants-2006_10
Patent number
US07119109B2

Reaction notes

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