Imidazole → HCID 22671917, compound

HRID 1637580Notes

Reaction equation

HRID 1637580 reaction equation
[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][OH:6].[Si:7](Cl)([C:10]([CH3:13])([CH3:12])[CH3:11])([CH3:9])[CH3:8].N1C=CN=C1.CN(C)C=[O:23]>CCCCCC>[Si:7]([O:6][CH:5]([OH:23])[CH2:4][CH2:3][CH2:2][Cl:1])([C:10]([CH3:13])([CH3:12])[CH3:11])([CH3:9])[CH3:8]

Participants

6

Reactant 4

HCID 795ImidazoleHCID 6228DimethylformamideHCID 135694-Chloro-1-butanolHCID 28928tert-Butyldimethylsilyl chloride

Product 1

HCID 22671917HCID 22671917, compoundYield 56%

Reagents, catalysts & solvents 1

HCID 8058HexaneSolvent

Procedure

4-Chloro-1-butanol (5.43 g, 50 mmol) was dissolved in dimethylformamide (50 mL) and tert-butyldimethylsilylchloride (7.54 g, 50 mmol) was added, followed by imidazole (3.4 g, 50 mmol). After 24 hours of stirring at room temperature, the reaction mixture was diluted with hexane, washed with water and brine and dried over anhydrous sodium sulfate. The solvent was evaporated to give colorless liquid which was purified by chromatography on silica gel eluting with hexanelethyl acetate (30:1) to give the product (7.26 g, 56%). 1H NMR (CDCl3) δ: 0.05 (s, 6H), 0.89 (s, 9 H), 1.64-1.68 (m, 2H), 1.82-1.86 (m, 2H), 3.57 (t, 2H), 3.64 (t, 2 H).

Workup

  1. washwashed with water and brine
  2. dry with materialdried over anhydrous sodium sulfate
  3. customThe solvent was evaporated
  4. customto give colorless liquid which
  5. customwas purified by chromatography on silica gel eluting with hexanelethyl acetate (30:1)

Sources & evidence

ORD record
ord-7c683290637d4a4680620bce7224ec6f
Source dataset
uspto-grants-2000_03
Patent number
US06043233

Reaction notes

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