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【结 构 式】

【分子编号】32941

【品名】5,7-bis(allyloxy)-2-[3-(allyloxy)-4-methoxyphenyl]-4H-chromen-4-one

【CA登记号】

【 分 子 式 】C25H24O6

【 分 子 量 】420.46196

【元素组成】C 71.42% H 5.75% O 22.83%

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)

The alkylation of diosmetin (I) with allyl bromide in the presence of NaH in DMF furnished the triallyl ether (II). Claisen rearrangement of (II) in refluxing trichlorobenzene then gave the title compound.

1 Wierzbicki, M.; Boussard, M.-F.; Verbeuren, T.; Vallez, M.-O.; Canet, E.; Rolland, Y. (ADIR et Cie.); Diosmetin derivs., process for their preparation and pharmaceutical compsns. containing them. CA 2161297; EP 0709383; FR 2726273; JP 1996225563; US 5629339 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
11463 3-Bromo-1-propene; 3-Bromopropene;allyl bromide 106-95-6 C3H5Br 详情 详情
(I) 30012 5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-chromen-4-one 520-34-3 C16H12O6 详情 详情
(II) 32941 5,7-bis(allyloxy)-2-[3-(allyloxy)-4-methoxyphenyl]-4H-chromen-4-one C25H24O6 详情 详情
Extended Information