Imidazole → 1-(2,5-Dimethoxy-3,4,6-trimethylbenzyl)imidazole

HRID 1030606Notes

Reaction equation

HRID 1030606 reaction equation
[NH:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.[CH3:6][O:7][C:8]1[C:15]([CH3:16])=[C:14]([CH3:17])[C:13]([O:18][CH3:19])=[C:12]([CH3:20])[C:9]=1[CH2:10]Br>CN(C)C=O.C(N(CC)CC)C.O>[CH3:19][O:18][C:13]1[C:14]([CH3:17])=[C:15]([CH3:16])[C:8]([O:7][CH3:6])=[C:9]([CH3:10])[C:12]=1[CH2:20][N:1]1[CH:5]=[CH:4][N:3]=[CH:2]1

Participants

6

Reactant 2

HCID 795ImidazoleHCID 142777601-(Bromomethyl)-2,5-dimethoxy-3,4,6-trimethylbenzene

Product 1

HCID 142777611-(2,5-Dimethoxy-3,4,6-trimethylbenzyl)imidazoleYield 47.3%

Reagents, catalysts & solvents 3

HCID 962WaterSolventHCID 6228DimethylformamideSolventHCID 8471TriethylamineSolvent

Procedure

To a solution of 499 mg (7.33 mmol) of imidazole and 2.0 g (7.33 mmol) of 2,5-dimethoxy-3,4,6-trimethylbenzyl bromide in 12 ml of dimethylformamide, 1.2 ml of triethylamine was added and stirred at room temperature for 1 hour. The reaction mixture was diluted with water and extracted with ethyl acetate. The extract was washed with water and dried, from which the solvent was evaporated off. The residue was purified with silica gel column chromatography (chloroform-methanol(1:1)) and recrystallized from isopropyl ether, to give 0.9 g (47.3%) of 1-(2,5-dimethoxy-3,4,6-trimethylbenzyl)imidazole. m.p. 82°-83° C.

Workup

  1. extractionextracted with ethyl acetate
  2. washThe extract was washed with water
  3. customdried, from which the solvent
  4. customwas evaporated off
  5. customThe residue was purified with silica gel column chromatography (chloroform-methanol(1:1))
  6. customrecrystallized from isopropyl ether

Sources & evidence

ORD record
ord-c9897c1639014373b74ccae6c4603ef5
Source dataset
uspto-grants-1992_04
Patent number
US05106858

Reaction notes

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