反应 #4153751
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-b08797dbc1b1416db51be7c3593bd6f2暂无可渲染的结构数据
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4-甲基戊酸(CAS 646-07-1)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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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b08797dbc1b1416db51be7c3593bd6f2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-473296d1fc664c1c92554b740ad09cae反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-65797f26c2f643cb9bd9b56a98ba342f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b43563937f414c6594fafe05a111dc99反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f9a590115b814f478845b3f330615d74反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6a295f1bf62b427b8bb361fd84047ff1反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c4ac6ef2103540e794ccd64403e63146反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d71ad6bcde594558b593c1b1712656bf反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Preparation of 2-(3-methyl-n-butyl)-indole. Carbonyldiimidazole (65 g) was mixed with 500 ml of dry dichloromethane in a 2-L round bottom flask and stirred magnetically. A solution of 4-methylvaleric acid in 200 ml of dichloromethane was added dropwise over 45 minutes and the mixture was stirred for another 1.25 hours. o-Toluidine (45 g) in 100 ml of dichloromethane was then added over about 20 minutes. After stirring for 2 hours the mixture was washed with water and then the solvent was stripped on a rotary evaporator. The residue was mixed with 150 ml of methanol and 75 ml of water and put in the freezer. Filtration of the precipitate, dilution of the filtrate with water and refiltration of the precipitate gave 75 g (94%) of vacuum dried N-(2-methylphenyl)-4-methylvaleramide which was used without further treatment in the next step. the mixture was stirred for another 1.25 hours After stirring for 2 hours the mixture was washed with water the solvent was stripped on a rotary evaporator The residue was mixed with 150 ml of methanol and 75 ml of water Filtration of the precipitate, dilution of the filtrate with water and refiltration of the precipitate
来源 ID: ord-9ed715a2df7c47048f4b78f4d6d76603反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound, white solid (77 mg, 73%), MS (ISP) m/z=427.4 [(M+H)+], mp 188° C., was prepared in accordance with the general method of example 1 from trans-4-{2-[4-(2,3-dihydro-benzofuran-4-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine dihydro chloride (intermediate B) (100 mg, 0.25 mmol) and 4-methyl-pentanoic acid.
来源 ID: ord-92788f0c3c3d4a70a739237458b56421反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b08797dbc1b1416db51be7c3593bd6f2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-473296d1fc664c1c92554b740ad09caePubChem References
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