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【结 构 式】 
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【分子编号】66856 【品名】(S)-ethyl 5-hydroxy-3-oxo-5-phenethyloctanoate 【CA登记号】 |
【 分 子 式 】C18H26O4 【 分 子 量 】306.40204 【元素组成】C 70.56% H 8.55% O 20.89% |
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：(VI)
| 【1】 Wilken J. Nerenz F, Kanschik-Conndsen A. 2004. A process for the synthesis of 3-hydroxy3-(2-phenylethyl) hexanoic acid，useful as an intermediate for antiviral. US 2004110957(本专利属于Honey-well International, Inc.，USA) |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| (V) | 21159 | (3R)-3-hydroxy-3-phenethylhexanoic acid | C14H20O3 | 详情 | 详情 | |
| (VII) | 66860 | (S)-4-hydroxy-6-phenethyl-6-propyl-5,6-dihydro-2H-pyran-2-one | C16H20O3 | 详情 | 详情 | |
| (I) | 17233 | 1-phenyl-3-hexanone | C12H16O | 详情 | 详情 | |
| (II) | 16640 | Ethyl 2-bromoacetate; Ethyl bromoacetate | 105-36-2 | C4H7BrO2 | 详情 | 详情 |
| (III) | 21156 | ethyl 3-hydroxy-3-phenethylhexanoate | C16H24O3 | 详情 | 详情 | |
| (IV) | 13355 | 2-Amino-1-phenyl-1-propanol; (1S,2R)-(+)-Norephedrine | 37577-28-9 | C9H13NO | 详情 | 详情 |
| (VI) | 66856 | (S)-ethyl 5-hydroxy-3-oxo-5-phenethyloctanoate | C18H26O4 | 详情 | 详情 | |
| (IX) | 17236 | (6R)-3-[(1R)-1-(3-aminophenyl)propyl]-4-hydroxy-6-phenethyl-6-propyl-5,6-dihydro-2H-pyran-2-one | C25H31NO3 | 详情 | 详情 |
Extended Information