【结 构 式】 |
【分子编号】29067 【品名】(E)-1-iodo-4-methyl-1-octen-4-ol 【CA登记号】 |
【 分 子 式 】C9H17IO 【 分 子 量 】268.13785 【元素组成】C 40.31% H 6.39% I 47.33% O 5.97% |
合成路线1
该中间体在本合成路线中的序号:(IV)The Grignard reaction of propargylmagnesium bromide (I) with 2-hexanone (II) in ether gives 4-methyloct-1-in-4-ol (III), which by reaction with diisobutylaluminum hydride and I2 is converted to 1-iodo-4-methyloct-1-en-4-ol (IV). The reaction of (IV) with dihydropyran and p-toluenesulfonic acid yields the corresponding tetrahydropyranyloxy derivative (V), which by reaction with tert-butyllithium and copper pentyne (VI) affords the corresponding organolithiocuprate (VII). The condensation of (VII) with 4R-(tetrahydropyranyloxy)-2-[7-(tetrahydropyranyloxyl)heptyl]cyclopent-2-en-1-one (VIII) in ether gives 1,11,16-tris(tetrahydropyranyloxy)-16-methylprost-13-en-9-one (IX), which is finally deprotected by a treatment with acetic acid in water THF.
【1】 Woessner, W.D.; Biddlecom, W.G.; Kluender, H.C. (Bayer Corp.); Preparation of 15-deoxy-16-hydroxyprostaglandins. US 4132738 . |
【2】 Castaner, J.; Serradell, M.N.; Rioprostil. Drugs Fut 1985, 10, 3, 207. |
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) | 29064 | bromo(2-propynyl)magnesium | C3H3BrMg | 详情 | 详情 | |
(II) | 29065 | 2-hexanone | 591-78-6 | C6H12O | 详情 | 详情 |
(III) | 29066 | 4-methyl-1-octyn-4-ol | C9H16O | 详情 | 详情 | |
(IV) | 29067 | (E)-1-iodo-4-methyl-1-octen-4-ol | C9H17IO | 详情 | 详情 | |
(V) | 29068 | (E)-2-butyl-5-iodo-2-methyl-4-pentenyl tetrahydro-2H-pyran-2-yl ether | C15H27IO2 | 详情 | 详情 | |
(VI) | 29069 | 1-pentynylcopper | C5H7Cu | 详情 | 详情 | |
(VIII) | 29070 | (4R)-4-[(tetrahydro-2H-pyran-2-yloxy)methyl]-2-[8-(tetrahydro-2H-pyran-2-yloxy)octyl]-2-cyclopenten-1-one | C24H40O5 | 详情 | 详情 | |
(IX) | 29071 | (2R,3S,4R)-3-[(E)-4-methyl-4-[(tetrahydro-2H-pyran-2-yloxy)methyl]-1-octenyl]-4-[(tetrahydro-2H-pyran-2-yloxy)methyl]-2-[8-(tetrahydro-2H-pyran-2-yloxy)octyl]cyclopentanone | C39H68O7 | 详情 | 详情 |