Imidazole → HCID 69733417、化合物
反応式
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][C:11]([F:14])([F:13])[F:12])=[C:6]([CH2:8][OH:9])[CH:7]=1.N1[CH:19]=[CH:18]N=C1.[Si:20](Cl)([C:23]([CH3:26])([CH3:25])[CH3:24])([CH3:22])[CH3:21]>CN(C=O)C>[Si:20]([O:9][CH2:8][C:6]1[CH:7]=[C:2]([NH:1][C:19]2[CH:18]=[CH:6][CH:7]=[CH:2][CH:3]=2)[CH:3]=[CH:4][C:5]=1[O:10][C:11]([F:12])([F:13])[F:14])([C:23]([CH3:26])([CH3:25])[CH3:24])([CH3:22])[CH3:21]参加物
5
実験手順
(5-Amino-2-trifluoromethoxyphenyl)methanol (1.2 g, 5.8 mmol) was dissolved in DMF (5 mL) and imidazole (0.48 g, 7.1 mmol) and tert-butyldimethylsilylchloride (0.99 g, 6.6 mmol) were added and the mixture was stirred for 16 hours. The reaction mixture was extracted with ethyl acetate (50 mL) and water (20 mL). The aqueous phase was extracted once more with ethyl acetate (20 mL). The combined organic phases were washed with water (10 mL), aqueous citric acid (10 mL, 10%) and water (2×10 mL), dried (magnesium sulphate) and concentrated in vacuo. The residue was purified by column chromatography (110 g, silica gel) using ethyl acetate and heptane (1:3) as eluent to give 1.2 g of 3-(tert-butyldimethylsilanyloxymethyl)-4-trifluoromethoxyphenylaniline.