Imidazole → HCID 12786200, compound

HRID 1449259Notes

Reaction equation

HRID 1449259 reaction equation
[I:1]/[CH:2]=[CH:3]/[CH2:4][C:5]([OH:11])([CH3:10])[CH2:6][CH2:7][CH2:8][CH3:9].N1C=CN=C1.CN(C)C=O.Cl[Si:23]([CH3:26])([CH3:25])[CH3:24]>CCCCCC>[I:1]/[CH:2]=[CH:3]/[CH2:4][C:5]([CH3:10])([O:11][Si:23]([CH3:26])([CH3:25])[CH3:24])[CH2:6][CH2:7][CH2:8][CH3:9]

Participants

6

Reactant 4

HCID 795ImidazoleHCID 6228DimethylformamideHCID 6397ChlorotrimethylsilaneHCID 12884304HCID 12884304, compound

Product 1

HCID 12786200HCID 12786200, compound

Reagents, catalysts & solvents 1

HCID 8058HexaneSolvent

Procedure

To a stirred mixture of 24.5 g (55.6 mmoles) of 1-iodo-4-hydroxy-4-methyl-trans-1-octene (Example 130), 13.6 g (200 mmoles) of imidazole, and 75 ml of dimethylformamide is added 10.9 g (100 moles) of chlorotrimethylsilane. After standing overnight the mixture is poured into 250 ml of hexane. The mixture is washed thoroughly with water followed by brine and dried over magnesium sulfate. After removal of the solvent, the product is distilled to give a colorless liquid, bp 67.5°-68° C. (0.07 mm).

Workup

  1. washThe mixture is washed thoroughly with water
  2. dry with materialdried over magnesium sulfate
  3. customAfter removal of the solvent
  4. distillationthe product is distilled
  5. customto give a colorless liquid, bp 67.5°-68° C. (0.07 mm)

Sources & evidence

ORD record
ord-db531645e29642e0b32d7c56f37da8ca
Source dataset
uspto-grants-1980_02
Patent number
US04189597

Reaction notes

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