Imidazole → 5-(t-Butyldimethylsiloxy)-3-pentyne

HRID 486176Notes

Reaction equation

HRID 486176 reaction equation
[CH2:1]([OH:5])[CH2:2][C:3]#[CH:4].[Si:6](Cl)([C:9]([CH3:12])([CH3:11])[CH3:10])([CH3:8])[CH3:7].N1C=CN=[CH:15]1>CN(C=O)C>[O:5]([CH2:1][C:2]#[C:3][CH2:4][CH3:15])[Si:6]([C:9]([CH3:12])([CH3:11])[CH3:10])([CH3:8])[CH3:7]

Participants

5

Reactant 3

HCID 795ImidazoleHCID 135663-Butyn-1-OLHCID 28928tert-Butyldimethylsilyl chloride

Product 1

HCID 110198575-(t-Butyldimethylsiloxy)-3-pentyne

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

To a solution of 3-butyn-1-ol (g) (10.0 g) in DMF (80 ml) were added t-butyldimethylsilyl chloride (21.5 g) and imidazol (10.6 g), and the resultant mixture was kept at 35° C. for 7 hours. The reaction mixture was treated in the conventional manner and the obtained crude product was distilled to give the title compound (h).

Workup

  1. additionThe reaction mixture was treated in the conventional manner
  2. customthe obtained crude product
  3. distillationwas distilled

Sources & evidence

ORD record
ord-e8abbd70f4304a4ab7461115c7d40f1a
Source dataset
uspto-grants-1994_03
Patent number
US05290811

Reaction notes

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