反应 #4163205
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-cce001ecb6464d4194ad58e3777750df暂无可渲染的结构数据
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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-cce001ecb6464d4194ad58e3777750df反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fad48856aab24aa3842a0a828e62bc36反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6f302f854bf0487c9f7ea3846844249d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ff1a59a9ecf54313afa78d8d2de76d5a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-96deb5b03472404c86f2762d7c916926反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-57e1d433ce0b46f9943eb45e98108a73反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Similarly prepared to Intermediate 1 from 1H-indazol-4-amine and ethyl 3-iodobenzoate.
来源 ID: ord-2a2cbc8bad1f451196ab06aae0f07762反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-cce001ecb6464d4194ad58e3777750df反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fad48856aab24aa3842a0a828e62bc36反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fad48856aab24aa3842a0a828e62bc36反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Magnesium (1.6 g) and p-bromotoluene (10.26 g) in 60 ml of tetrahydrofuran were stirred and warmed until the reaction commenced. When the exothermic reaction had finished, the mixture was refluxed overnight. In a separate flask, 4 ml of DIBAL (1M in toluene) was added to a suspension of bis(triphenylphosphine)palladium(II) chloride (1.4 g) in 100 ml of tetrahydrofuran, followed by ethyl 3-iodobenzoate (11.04 g). To this mixture, the magnesium reagent prepared above was added dropwise, causing an exothermic reaction. The reaction mixture was stirred overnight at room temperature, and then quenched by addition of dilute hydrochloric acid. The mixture was extracted with ether, and the organic layer washed with water, and then saturated brine. The organic layer was separated, dried over sodium sulfate, the solvent evaporated under reduced pressure, and the residue chromatographed on silica gel, eluting with 5% ethyl acetate in heptane, to yield 5.69 g of ethyl 4'-methylbiphenyl-3-carboxylate, a compound of Formula (17), as a pale yellow oil. warmed until the reaction commenced When the exothermic reaction the mixture was refluxed overnight above was added dropwise an exothermic reaction quenched by addition of dilute hydrochloric acid The mixture was extracted with ether the organic layer washed with water The organic layer was separated dried over sodium sulfate the solvent evaporated under reduced pressure the residue chromatographed on silica gel eluting with 5% ethyl acetate in heptane
来源 ID: ord-35c48f52b06d4ec986257d5697e09ada反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Magnesium (1.6 g) and p-bromotoluene (10.26 g) in 60 ml of tetrahydrofuran were stirred and warmed until the reaction commenced. When the exothermic reaction had finished, the mixture was refluxed overnight. In a separate flask, 4 ml of DIBAL (1M in toluene) was added to a suspension of bis(triphenylphosphine)palladium(II) chloride (1.4 g) in 100 ml of tetrahydrofuran, followed by ethyl 3-iodobenzoate (11.04 g). To this mixture, the magnesium reagent prepared above was added dropwise, causing an exothermic reaction. The reaction mixture was stirred overnight at room temperature, and then quenched by addition of dilute hydrochloric acid. The mixture was extracted with ether, and the organic layer washed with water, and then saturated brine. The organic layer was separated, dried over sodium sulfate, the solvent evaporated under reduced pressure, and the residue chromatographed on silica gel, eluting with 5% ethyl acetate in heptane, to yield 5.69 g of ethyl 4'-methylbiphenyl-3-carboxylate, a compound of Formula (17), as a pale yellow oil. warmed until the reaction commenced When the exothermic reaction the mixture was refluxed overnight above was added dropwise an exothermic reaction quenched by addition of dilute hydrochloric acid The mixture was extracted with ether the organic layer washed with water The organic layer was separated dried over sodium sulfate the solvent evaporated under reduced pressure the residue chromatographed on silica gel eluting with 5% ethyl acetate in heptane
来源 ID: ord-35c48f52b06d4ec986257d5697e09adaPubChem References
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