Pyridine → (But-3-yn-1-yloxy)(tert-butyl)dimethylsilane

HRID 1275116Notes

Reaction equation

HRID 1275116 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=CC=CC=1>C(Cl)Cl>[Si:6]([O:5][CH2:1][CH2:2][C:3]#[CH:4])([C:9]([CH3:12])([CH3:11])[CH3:10])([CH3:8])[CH3:7]

Participants

5

Procedure

To a solution of 3-butyne-1-ol (5.0 g; 71.3 mmol) in ca. 75 ml of methylene chloride was added tert-butydimethylsilyl chloride (10.8 g; 71.6 mmol) and 7 ml of pyridine. The mixture was allowed to stir overnight at room temperature, diluted with methylene chloride, washed with water, 1M HCl, brine and dried (Na2SO4). Concentration in vacuo afforded the title compound as a colorless liquid.

Workup

  1. washwashed with water, 1M HCl, brine
  2. dry with materialdried (Na2SO4)
  3. concentrationConcentration in vacuo

Sources & evidence

ORD record
ord-a2472a96116e417899b81f7cc0ae58dd
Source dataset
uspto-grants-2000_12
Patent number
US06160000

Reaction notes

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