[CH3:1][CH:2]([CH2:18][CH3:19])[CH2:3][O:4]C1C=CC(C2C=CC(O)=CC=2)=CC=1.CC(CC)CO[C:24]1[CH:29]=[CH:28][C:27]([C:30]2[CH:35]=[CH:34][C:33]([OH:36])=[C:32]([Br:37])[CH:31]=2)=[CH:26][CH:25]=1.BrBr>O1CCOCC1>[CH3:1][CH:2]([CH2:18][CH3:19])[CH2:3][O:4][C:31]1[C:32]([Br:37])=[C:33]([OH:36])[CH:34]=[CH:35][C:30]=1[C:27]1[CH:26]=[CH:25][CH:24]=[CH:29][CH:28]=14'-(2-Methylbutyloxy)-4-hydroxybiphenyl (15 g) obtained in Example 1, (i) was dissolved in 1,4-dioxane (50 ml), followed by dropwise adding a mixture of bromine (10.5 g) and 1,4-dioxane (140 ml), heating on a water bath at 40° C. for 4 hours with stirring, thereafter distilling off 1,4-dioxane under reduced pressure, adding toluene (300 ml) to the remaining solution, adding a 10% aqueous solution of sodium hydrogen sulfite till the color of bromine disappeared, three times washing with saturated aqueous solution of NaCl to make the liquid neutral, drying and distilling off toluene to obtain a raw product of 4'-(2-methylbutyloxy-3-bromo-4-hydroxybiphenyl (21 g).
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