【结 构 式】 |
【分子编号】62341 【品名】2,6-di(tert-butyl)-4-(methoxymethyl)phenol 【CA登记号】 |
【 分 子 式 】C16H26O2 【 分 子 量 】250.38124 【元素组成】C 76.75% H 10.47% O 12.78% |
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:(IX)In a further method, condensation of benzyl alcohol (III) with methanol in the presence of a catalytic amount of HCl afforded the corresponding methyl ether (IX), which was then reacted with diphosphonate (I) in the presence of NaH to furnish the target arylethyl diphosphonate (1). Optionally, diphosphonate (I) was condensed with the benzyl acetate ester (X), prepared from benzyl chloride (II) and potassium acetate in acetone
【1】 Grinter, T.J.; Harris, M.A.; Hayler, J.D.; Negus, A. (Ilex Oncology Research-Europe SA); A process for the preparation of diphosphonate derivs.. WO 9731004 . |
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) | 27980 | Diisopropyl (diisopropoxyphosphoryl)methylphosphonate; Tetraisopropyl methylenediphosphonate | 1660-95-3 | C13H30O6P2 | 详情 | 详情 |
(II) | 62335 | 2,6-di(tert-butyl)-4-(chloromethyl)phenol | C15H23ClO | 详情 | 详情 | |
(III) | 37706 | 2,6-di(tert-butyl)-4-(hydroxymethyl)phenol | 88-26-6 | C15H24O2 | 详情 | 详情 |
(IX) | 62341 | 2,6-di(tert-butyl)-4-(methoxymethyl)phenol | C16H26O2 | 详情 | 详情 | |
(X) | 62342 | 3,5-di(tert-butyl)-4-hydroxybenzyl acetate | C17H26O3 | 详情 | 详情 |
Extended Information