Methyl iodide → 5-methyl-1-(4-vinylphenyl)-1H-1,2,4-triazole
反応式
[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]=1参加物
実験手順
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.
後処理
- 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)
出典と根拠
- ORDレコード
- ord-474551fe3c484ef5964358c084ba6aca
- 出典データセット
- uspto-grants-2015_12
- 特許番号
- US09210927B2
反応ノート
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