Imidazole → 4-(4-Methylphenyl)butyl tert-butyldimethylsilyl ether

HRID 1751856Notes

Reaction equation

HRID 1751856 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][CH2:11][OH:12])=[CH:4][CH:3]=1.N1C=CN=C1.[Si:18](Cl)([C:21]([CH3:24])([CH3:23])[CH3:22])([CH3:20])[CH3:19]>CN(C=O)C>[Si:18]([O:12][CH2:11][CH2:10][CH2:9][CH2:8][C:5]1[CH:6]=[CH:7][C:2]([CH3:1])=[CH:3][CH:4]=1)([C:21]([CH3:24])([CH3:23])[CH3:22])([CH3:20])[CH3:19]

Participants

5

Reactant 3

HCID 795ImidazoleHCID 28928tert-Butyldimethylsilyl chlorideHCID 1040094-(4-Methylphenyl)butanol

Product 1

HCID 596786264-(4-Methylphenyl)butyl tert-butyldimethylsilyl ether

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

4-(4-Methylphenyl)butanol (0.5 g, 3.04 mmol) is dissolved in 5 ml DMF and to it is added imidazole (310 mg, 4.56 mmol) and tert-butyldimethylsilyl chloride (685 mg, 4.56 mmol). The reaction is stirred for 4 hrs after which it is extracted in ethyl acetate and washed with water to remove all DMF. The organic layer is then dried and concentrated. The crude mixture is then purified by flash chromatography using a mixture of ethyl acetate-hexanes as the eluting medium to afford the above mentioned product.

Workup

  1. extractionis extracted in ethyl acetate
  2. washwashed with water
  3. customto remove all DMF
  4. customThe organic layer is then dried
  5. concentrationconcentrated
  6. customThe crude mixture is then purified by flash chromatography
  7. additiona mixture of ethyl acetate-hexanes as the eluting medium
  8. customto afford the

Sources & evidence

ORD record
ord-434e0339595247bf9390286c5773cd95
Source dataset
uspto-grants-2015_10
Patent number
US09161997B2

Reaction notes

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