Imidazole → (4R)-4-(2-iodoethyl)-2,2-dimethyl-1,3-dioxolane

HRID 1847068Notes

Reaction equation

HRID 1847068 reaction equation
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N1C=CN=C1.[I:25]I.O[CH2:28][CH2:29][C@@H:30]1[CH2:34][O:33][C:32]([CH3:36])([CH3:35])[O:31]1.S([O-])([O-])(=O)=S.[Na+].[Na+]>C(OCC)C.C(#N)C>[I:25][CH2:28][CH2:29][C@@H:30]1[CH2:34][O:33][C:32]([CH3:36])([CH3:35])[O:31]1

Participants

7

Procedure

Triphenyl phosphine (5.94 g, 22.65 mmol) and imidazole (22.65 mmol) were dissolved in a mixed solution (120 ml) of diethyl ether-acetonitrile (3:1). Iodine (5.75 g, 22.65 mmol) was added thereto under cooling on ice and the mixture was stirred at room temperature for 30 minutes. The solution was cooled on ice again, (4R)-4-(2-hydroxyethyl)-2,2-dimethyl-1,3-dioxolane (3.0 mmol, 20.59 mmol) was added thereto and the mixture was stirred at room temperature for 24 hours. A saturated sodium thiosulfate aqueous solution was added to the reaction solution under cooling on ice and stirred for a while, the solution was extracted with diethyl ether and the extract was washed with saturated sodium chloride solution. The solvent was removed under reduced pressure and the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to yield 3.20 g (61%) of the title compound in the form of a yellowish oily product.

Workup

  1. temperatureunder cooling on ice
  2. temperatureThe solution was cooled on ice again
  3. stirringthe mixture was stirred at room temperature for 24 hours
  4. temperatureunder cooling on ice
  5. stirringstirred for a while
  6. extractionthe solution was extracted with diethyl ether
  7. washthe extract was washed with saturated sodium chloride solution
  8. customThe solvent was removed under reduced pressure
  9. customthe residue was purified by silica gel column chromatography (hexane/ethyl acetate)

Sources & evidence

ORD record
ord-e0747f819a9c48538a1f768b8e57b0b3
Source dataset
uspto-grants-2015_02
Patent number
US08952010B2

Reaction notes

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