Imidazole → [(4-Cyclopropyloct-1-yn-4-yl)oxy](trimethyl)silane

HRID 2057835Notes

Reaction equation

HRID 2057835 reaction equation
[CH:1]1([C:4]([OH:12])([CH2:8][CH2:9][CH2:10][CH3:11])[CH2:5][C:6]#[CH:7])[CH2:3][CH2:2]1.N1C=CN=C1.Cl[Si:19]([CH3:22])([CH3:21])[CH3:20]>CN(C)C=O>[CH:1]1([C:4]([O:12][Si:19]([CH3:22])([CH3:21])[CH3:20])([CH2:8][CH2:9][CH2:10][CH3:11])[CH2:5][C:6]#[CH:7])[CH2:2][CH2:3]1

Participants

5

Reactant 3

HCID 795ImidazoleHCID 6397ChlorotrimethylsilaneHCID 130787514-Cyclopropyl-4-hydroxy-1-octyne

Product 1

HCID 13078752[(4-Cyclopropyloct-1-yn-4-yl)oxy](trimethyl)silane

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

To a stirred solution of 27.8 g of 4-cyclopropyl-4-hydroxy-1-octyne (Example 190) and 33.3 g of imidazole in 130 ml of dimethylformamide at 5° C. is added 24 ml of chlorotrimethylsilane during 5 minutes. The solution is stirred at ambient temperature for 17 hours and then partitioned with 600 ml of hexane and 250 ml of ice water. The hexane phase is separated and washed successively with water and brine. The solution is dried over magnesium sulfate and evaporated to give a liquid, pmr spectrum (CDCl3): δ 0.12 (singlet, trimethylsiloxy group), 2.02 (triplet, HC≡C), and 2.45 (doublet, C≡CH2).

Workup

  1. custompartitioned with 600 ml of hexane and 250 ml of ice water
  2. customThe hexane phase is separated
  3. washwashed successively with water and brine
  4. dry with materialThe solution is dried over magnesium sulfate
  5. customevaporated
  6. customto give a liquid, pmr spectrum (CDCl3)

Sources & evidence

ORD record
ord-14f281c00de8431e8ae380fccf77428a
Source dataset
uspto-grants-1980_07
Patent number
US04212969

Reaction notes

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