Imidazole → (3-Iodo-1-trifluoromethylpropyl)-benzene

HRID 885158Notes

Reaction equation

HRID 885158 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:40])([F:39])[CH:29]([C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)[CH2:30][CH2:31]O>ClCCl>[I:25][CH2:31][CH2:30][CH:29]([C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)[C:28]([F:40])([F:39])[F:27]

Participants

6

Procedure

To a stirred solution of triphenylphosphine (3.93 g) and imidazole (1.02 g) in dichloromethane (20 ml) under an argon atmosphere was added slowly iodine (3.81 g) and rac-4,4,4-trifluoro-3-phenyl-butan-1-ol (2.04 g, CAS 65948-16-5). The mixture was stirred for 2 hours at room temperature, then dichloromethane (50 ml) was added and mixture was extracted with saturated sodium thiosulfate solution (50 ml) and hydrochloric acid (1N, 25 ml). The organic layer was dried over MgSO4 and evaporated. The residue was suspended in ether and filtered to remove insoluble triphenylphosphine oxide. The ether was evaporated and the residue was purified by column chromatography (SiO2, heptane/EtOAc=9:1) to yield a light yellow liquid, (1.99 g, 63%).

Workup

  1. extractionmixture was extracted with saturated sodium thiosulfate solution (50 ml) and hydrochloric acid (1N, 25 ml)
  2. dry with materialThe organic layer was dried over MgSO4
  3. customevaporated
  4. filtrationfiltered
  5. customto remove insoluble triphenylphosphine oxide
  6. customThe ether was evaporated
  7. customthe residue was purified by column chromatography (SiO2, heptane/EtOAc=9:1)
  8. customto yield a light yellow liquid, (1.99 g, 63%)

Sources & evidence

ORD record
ord-732db728c5334ce98790201c29f5a43c
Source dataset
uspto-grants-2012_08
Patent number
US08242153B2

Reaction notes

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