反应 #4119166
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4d76aee59e384c1d9974e6168d8cef28暂无可渲染的结构数据
C1CCC2C(C1)CCCC2=O产品信息
1-萘烷酮(CAS 4832-16-0)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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合成路线数据
7 条反应 · 7 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4d76aee59e384c1d9974e6168d8cef28反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6c05f5ed13624f62b8d6b7d43ac4d5f7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 64 parts of octahydro-1(2H)-naphthalenone, 50 parts of methyl glycine hydrochloride, 2 parts of a solution of thiophene in methanol 4%, 560 parts of methanol and 50 parts of potassium acetate was hydrogenated at normal pressure and at room temperature with 5 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was taken up in a mixture of water and trichloromethane. The whole was treated with a sodium hydroxide solution. The separated organic layer was dried, filtered and evaporated, yielding 82.2 parts (91.1%) of methyl N-(decahydro-1-naphthalenyl)glycine as a residue (intermediate 1). the catalyst was filtered off the filtrate was evaporated The residue was taken up in a mixture of water and trichloromethane The whole was treated with a sodium hydroxide solution The separated organic layer was dried filtered evaporated
来源 ID: ord-7c9eacba54b14dbc9c848641b1f7f478反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4d76aee59e384c1d9974e6168d8cef28反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6c05f5ed13624f62b8d6b7d43ac4d5f7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A suspension of sodium hydride (4.60 g, 115 mmol) in tetrahydrofuran (20 mL) was treated with dimethyl carbonate (8.29 mL, 99 mmol), heated to reflux under nitrogen, treated dropwise with a solution of octahydronaphthalen-1(2H)-one (Aldrich cat#115063, mixture of trans (major) and cis (minor), 5 g, 32.8 mmol) in tetrahydrofuran (20 mL) over 5 minutes, and heated to reflux overnight. The mixture was cooled, diluted with ether (300 mL) and treated with 1 M hydrochloric acid (150 mL). The layers were separated and the aqueous layer was extracted with ether (2×100 mL). The combined ether layers were washed with brine, dried (magnesium sulfate), filtered and concentrated to provide the desired product that was not purified, but used as is in the next step. heated to reflux under nitrogen heated to reflux overnight The mixture was cooled The layers were separated the aqueous layer was extracted with ether (2×100 mL) The combined ether layers were washed with brine dried (magnesium sulfate) filtered concentrated
来源 ID: ord-9e5624f377624a6cbff153162646725b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 64 parts of octahydro-1(2H)-naphthalenone, 50 parts of methyl glycine hydrochloride, 2 parts of a solution of thiophene in methanol 4%, 560 parts of methanol and 50 parts of potassium acetate was hydrogenated at normal pressure and at room temperature with 5 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was taken up in a mixture of water and trichloromethane. The whole was treated with a sodium hydroxide solution. The separated organic layer was dried, filtered and evaporated, yielding 82.2 parts (91.1%) of methyl N-(decahydro-1-naphthalenyl)glycine as a residue (intermediate 1). the catalyst was filtered off the filtrate was evaporated The residue was taken up in a mixture of water and trichloromethane The whole was treated with a sodium hydroxide solution The separated organic layer was dried filtered evaporated
来源 ID: ord-7c9eacba54b14dbc9c848641b1f7f478PubChem References
以下资料来自该化合物的公开数据库参考记录。
