反应 #3868223
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-227fe1b32637433d87e22ac74c82e3e8暂无可渲染的结构数据
CC1=CC=C(C=C1)CCCCBr产品信息
1-(4-溴丁基)-4-甲基苯(CAS 99857-43-9)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
4 条反应 · 4 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-227fe1b32637433d87e22ac74c82e3e8反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Phenylmalonic acid diethyl ester (8.8 mmol) dissolved in 5 ml absolute tetrahydrofuran is added dropwise to 20 ml absolute tetrahydrofuran and sodium hydride (9.7 mmol). Then 4-p-tolylbutyl bromide (8.8 mmol) dissolved in 10 ml absolute tetrahydrofuran is added after 15 minutes. It is heated for 3 days under reflux. The solvent is concentrated in a vacuum. The residue is taken up in 50 ml ethyl acetate and extracted with 2×50 ml water. The organic phase is dried over magnesium sulfate, filtered and concentrated by evaporation. It is purified by chromatography on silica gel (heptane/ethyl acetate 9:1). Yield 55% colourless oil. is added after 15 minutes It is heated for 3 days under reflux The solvent is concentrated in a vacuum extracted with 2×50 ml water The organic phase is dried over magnesium sulfate filtered concentrated by evaporation It is purified by chromatography on silica gel (heptane/ethyl acetate 9:1)
来源 ID: ord-734850e9383848738f23e0464fb11f1b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Phenylmalonic acid diethyl ester (8.8 mmol) dissolved in 5 ml absolute tetrahydrofuran is added dropwise to 20 ml absolute tetrahydrofuran and sodium hydride (9.7 mmol). Then 4-p-tolylbutyl bromide (8.8 mmol) dissolved in 10 ml absolute tetrahydrofuran is added after 15 minutes. It is heated for 3 days under reflux. The solvent is concentrated in a vacuum. The residue is taken up in 50 ml acette and extracted with 2×50 ml water. The organic phase is dried over magnesium sulfate, filtered and concentrated by evaporation. It is purified by chromatography on silica gel (heptane/ethyl acetate 9:1). Yield 55% colouriess oil. is added after 15 minutes It is heated for 3 days under reflux The solvent is concentrated in a vacuum extracted with 2×50 ml water The organic phase is dried over magnesium sulfate filtered concentrated by evaporation It is purified by chromatography on silica gel (heptane/ethyl acetate 9:1)
来源 ID: ord-254baf31a1684e93b0690ee94435397e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Phenylmalonic acid diethyl ester (8.8 mmol) dissolved in 5 ml absolute tetrahydrofuran is added dropwise to 20 ml absolute tetrahydrofuran and sodium hydride (9.7 mmol). Then 4-p-tolylbutyl bromide (8.8 mmol) dissolved in 10 ml absolute tetrahydrofuran is added after 15 minutes. It is heated for 3 days under reflux. The solvent is concentrated in a vacuum. The residue is taken up in 50 ml ethyl acetate and extracted with 2×50 ml water. The organic phase is dried over magnesium sulfate, filtered and concentrated by evaporation. It is purified by chromatography on silica gel (heptane/ethyl acetate 9:1). Yield 55% colourless oil. is added after 15 minutes It is heated for 3 days under reflux The solvent is concentrated in a vacuum extracted with 2×50 ml water The organic phase is dried over magnesium sulfate filtered concentrated by evaporation It is purified by chromatography on silica gel (heptane/ethyl acetate 9:1)
来源 ID: ord-734850e9383848738f23e0464fb11f1bPubChem References
以下资料来自该化合物的公开数据库参考记录。
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