Imidazole → Tert-butyl((2-iodoallyl)oxy)dimethylsilane

HRID 1852842Notes

Reaction equation

HRID 1852842 reaction equation
[I:1][C:2](=[CH2:5])[CH2:3][OH:4].N1C=CN=C1.[Si:11](Cl)([C:14]([CH3:17])([CH3:16])[CH3:15])([CH3:13])[CH3:12]>ClCCl>[C:14]([Si:11]([O:4][CH2:3][C:2]([I:1])=[CH2:5])([CH3:13])[CH3:12])([CH3:17])([CH3:16])[CH3:15]

Participants

5

Procedure

A stirred solution of 2-iodoprop-2-en-1-ol (24 g, 130.4 mmol) in dry dichloromethane (500 mL) was cooled to 0° C. Imidazole (17.75 g, 260.9 mmol) was added in several portions, and the mixture was stirred for 10 minutes. Tert-butyldimethylsilyl chloride (29.49 g, 195.9 mmol) was added in several portions at 0° C., and the reaction mixture was slowly warmed to room temperature and stirred for 3 h. The reaction mixture was quenched with water (100 mL), and the organic phase was separated. The organic phase was washed with brine (100 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure (water bath temperature <25° C.). The residue was purified by column chromatography using 100% petroleum ether as eluent to afford tert-butyl((2-iodoallyl)oxy)dimethylsilane.

Workup

  1. stirringstirred for 3 h
  2. customThe reaction mixture was quenched with water (100 mL)
  3. customthe organic phase was separated
  4. washThe organic phase was washed with brine (100 mL)
  5. dry with materialdried over anhydrous Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure (water bath temperature <25° C.)
  8. customThe residue was purified by column chromatography

Sources & evidence

ORD record
ord-f8e2da741ed4416680765d67425365b9
Source dataset
uspto-grants-2015_02
Patent number
US08962611B2

Reaction notes

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