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【结 构 式】

【分子编号】37073

【品名】1-[3-allyl-2-hydroxy-6-(2-hydroxypropoxy)phenyl]-1-ethanone

【CA登记号】

【 分 子 式 】C14H18O4

【 分 子 量 】250.29452

【元素组成】C 67.18% H 7.25% O 25.57%

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:(I)

The hydrogenation of 2-hydroxy-3-allyl-6-(2-hydroxypropoxy)acetophenone (I) with H2 over Pd/C in ethanol gives 2-hydroxy-3-propyl-6-(2-hydroxypropoxy)acetophenone (II), which is then cyclized with diethyl oxalate (III) by means of sodium ethoxide in refluxing ethanol. The sodium salt is prepared by treatment of the acid with NaHCO3 in water.

1 Cairns, H.; Hazard, R.; King, J.; Lee, T.B.; DE 2530289 .
2 Sneddon, J.M.; Serradell, M.N.; Castaner, J.; Blancafort, P.; FPL-52,694. Drugs Fut 1982, 7, 6, 388.
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) 37073 1-[3-allyl-2-hydroxy-6-(2-hydroxypropoxy)phenyl]-1-ethanone C14H18O4 详情 详情
(II) 37074 1-[2-hydroxy-6-(2-hydroxypropoxy)-3-propylphenyl]-1-ethanone C14H20O4 详情 详情
(III) 17571 Diethyl oxalate; Ethyl 2-ethoxy-2-oxoacetate 95-92-1 C6H10O4 详情 详情
Extended Information