Methyl Salicylate → HCID 67549718、化合物
反応式
[C:1]([O:10][CH3:11])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)O.C(O)[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23].[CH3:25][O:26][C:27]([C:29]1[CH:30]=[CH:31]C(O)=[CH:33][CH:34]=1)=[O:28].C(C(CCCCCC)CO)CCC>>[C:1]([O:10][C:11]1[CH:31]=[CH:30][C:29]([C:27]([O:26][CH2:25][CH:17]([CH2:16][CH2:15][CH2:14][CH3:13])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])=[O:28])=[CH:34][CH:33]=1)(=[O:9])[C:2]1[CH:3]=[CH:5][CH:6]=[CH:7][CH:8]=1参加物
5
実験手順
In place of 25 g of methyl salicylate and 31 g of n-dodecanol in Example 1-6, 25 g of methyl p-hydroxybenzoate and 31 g of 2-butyl octanol were used for preparation in the same manner in Example 1-6 to obtain 48 g of 2-butyloctyl p-benzoyloxybenzoate.