Methyl iodide → 5-methyl-1-(4-vinylphenyl)-1H-1,2,4-triazole
Reaction equation
[CH:1]([C:3]1[CH:8]=[CH:7][C:6]([N:9]2[CH:13]=[N:12][CH:11]=[N:10]2)=[CH:5][CH:4]=1)=[CH2:2].[Li][CH2:15]CCC.CI>C1COCC1>[CH3:15][C:13]1[N:9]([C:6]2[CH:5]=[CH:4][C:3]([CH:1]=[CH2:2])=[CH:8][CH:7]=2)[N:10]=[CH:11][N:12]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred solution of 1-(4-vinyl-phenyl)-1H-[1,2,4]triazole (0.5 g, 2.9 mmol) in 10 mL of THF, was added n-BuLi (0.22 g, 3.5 mmol) at −78° C. and stirred for 30 min. To this methyl iodide in THF (0.50 g, 3.5 mmol) was added and the resultant reaction mixture was stirred at ambient temperature for 16 h. The reaction mixture was quenched with a saturated aqueous NH4Cl solution and extracted with EtOAc (3×25 mL). The combined EtOAc layer was washed with brine and dried over sodium sulphate and concentrated under reduced pressure The crude compound was purified by flash chromatography (SiO2, 100-200 mesh, 40% EtOAc in Pet ether) afford the title compound as a pale brown liquid (250 mg, 46%): 1H NMR (400 MHz, CDCl3) δ 7.93 (s, 1H), 7.55 (d, J=9 Hz, 2H), 7.42 (d, J=9 Hz, 2H), 6.76 (dd, J=18, 11 Hz, 1H), 5.83 (d, J=18 Hz, 1H), 5.38 (d, J=11 Hz, 1H), 2.55 (s, 3H); ESIMS m/z 186.13 ([M+H]+); IR (thin film) 1517, 1386, 1182, 847 cm−1.
Workup
- customthe resultant reaction mixture
- stirringwas stirred at ambient temperature for 16 h
- customThe reaction mixture was quenched with a saturated aqueous NH4Cl solution
- extractionextracted with EtOAc (3×25 mL)
- washThe combined EtOAc layer was washed with brine
- dry with materialdried over sodium sulphate
- concentrationconcentrated under reduced pressure The crude compound
- customwas purified by flash chromatography (SiO2, 100-200 mesh, 40% EtOAc in Pet ether)
Sources & evidence
- ORD record
- ord-17dee33ec91b4d119b38f0cc577c36bc
- Source dataset
- uspto-grants-2016_01
- Patent number
- US09226500B2
Reaction notes
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