【结 构 式】 |
【分子编号】47148 【品名】ethyl 2,4-dihydroxy-3,6-dimethylbenzoate 【CA登记号】 |
【 分 子 式 】C11H14O4 【 分 子 量 】210.22976 【元素组成】C 62.85% H 6.71% O 30.44% |
与该中间体有关的原料药合成路线共 1 条
合成路线1
该中间体在本合成路线中的序号:(II)Ethyl ester (II) is alkylated with benzyl chloride (I) by means of K2CO3 in acetone to yield 4-benzyloxy derivative (III), which is then hydrolyzed with KOH in H2O/DMSO to provide carboxylic acid (IV). Depside formation between derivative (IV) and ethyl ester (II) by means of trifluoroacetic anhydride in toluene furnishes ethyl benzoate derivative (V), which is finally hydrogenated over Pd/C in AcOEt to yield the target product.
【1】 Kumar, S.; Muller, K.; Depsides as non-redox inhibitors of leukotriene B4 biosynthesis and HaCaT cell growth. 1.Novel analogues of barbatic and diffractaic acid. Eur J Med Chem 1999, 34, 12, 1035. |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(I) | 19171 | 1-(Chloromethyl)benzene; Benzyl chloride | 100-44-7 | C7H7Cl | 详情 | 详情 |
(II) | 47148 | ethyl 2,4-dihydroxy-3,6-dimethylbenzoate | C11H14O4 | 详情 | 详情 | |
(III) | 47149 | ethyl 4-(benzyloxy)-2-hydroxy-3,6-dimethylbenzoate | C18H20O4 | 详情 | 详情 | |
(IV) | 47150 | 4-(benzyloxy)-2-hydroxy-3,6-dimethylbenzoic acid | C16H16O4 | 详情 | 详情 | |
(V) | 47151 | ethyl 4-[[4-(benzyloxy)-2-hydroxy-3,6-dimethylbenzoyl]oxy]-2-hydroxy-3,6-dimethylbenzoate | C27H28O7 | 详情 | 详情 |
Extended Information