[CH3:1][C:2]([CH3:21])=[CH:3][CH2:4][CH2:5][C:6]1[CH2:11][CH2:10][CH:9]([CH2:12][CH2:13][C:14]2[CH:19]=[CH:18][C:17](O)=[CH:16][CH:15]=2)[CH2:8][CH:7]=1.S([C:26]1[CH:32]=[CH:31][C:29]([CH3:30])=[CH:28][CH:27]=1)([O-])(=O)=O.[C:33](=[O:36])([O-])[O-].[Cs+].[Cs+].Cl>CN(C)C=O>[CH3:1][C:2]([CH3:21])=[CH:3][CH2:4][CH2:5][C:6]1[CH2:11][CH2:10][CH:9]([CH2:12][CH2:13][C:14]2[CH:19]=[CH:18][C:17]([O:36][CH2:33][CH:26]3[CH2:32][CH2:31][C:29]([CH2:30][CH2:1][CH2:2][CH2:3][CH3:4])=[CH:28][CH2:27]3)=[CH:16][CH:15]=2)[CH2:8][CH:7]=1To a round-bottom flask equipped with a stirbar is added phenol 2G (R=4-Methyl-3-pentenyl) (5 g), tosylate 1H (R=n-pentyl) (5.95 g), cesium carbonate (7.45 g), and anhydrous dimethylforrnamide (50 mL). The reaction mixture is stirred overnight. It is then poured into 50 mL dilute HCl, and extracted with 1:1 hexanes:ethyl acetate. The combined organic layers are washed with brine and dried over potassium carbonate, and the solution is concentrated in vacuo. Filtration through silica gel using 10% ethyl acetate in hexanes gives the pure product.
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