反应 #4173759
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openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-557e42a1d886475ebf7189ffa83cdec9暂无可渲染的结构数据
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2-丁炔-1,4-二醇(CAS 110-65-6)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-557e42a1d886475ebf7189ffa83cdec9反应条件: temp:0.00; pressure:0.00; stir:
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来源 ID: ord-e52fde4fc9fc441ea31b28ec77bb878a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-56787166effd4798b55654e55fa173c0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-878493b369e44c549ba8c62834f7c89d反应条件: temp:0.00; pressure:0.00; stir:
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来源 ID: ord-2364be28b11246f4a943e3e654da9ce5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-19ae4076a0b84c7d846593418efcf897反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a9c5478a45194ce7bfdb15e3fe11b28b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8c85404dd01e4253905d8b70ee786344反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Sodium hydride (60% dispersion in oil, 7.5 g, 188 mmol) was added to a solution of 2-butyne-1,4-diol (16.1 g, 187 mmol) in THF (150 mL) at 0° C. under nitrogen. After 1 h at 0° C., bromoacetonitrile (8.33 mL, 120 mmol) was added slowly and the reaction was allowed to warm to rt. After 22 h at rt, the reaction was quenched with 1 N HCl (150 mL) and extracted with EtOAc (3×150 mL). The combined extracts were washed with brine (150 mL), dried (Na2SO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (CH2Cl2→2% MeOH/CH2Cl2, gradient) afforded 4.35 g (29%) of (4-hydroxy-but-2-ynyloxy)-acetonitrile. After 22 h at rt the reaction was quenched with 1 N HCl (150 mL) extracted with EtOAc (3×150 mL) The combined extracts were washed with brine (150 mL) dried (Na2SO4) filtered concentrated in vacuo Purification of the residue by flash column chromatography on silica gel (CH2Cl2→2% MeOH/CH2Cl2, gradient)
来源 ID: ord-a0263dc918064c5f93fc19fbc61dc920反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Sodium hydride (60% dispersion in oil, 2.32 g, 58 mmol) was added to a solution of 2-butyne-1,4-diol (5.0 g, 58 mmol) in THF (60 mL) at 0° C. under nitrogen. After 1 h at 0° C., methyl bromomethylacetate (5.5 mL, 58 mmol) was added and the reaction was allowed to warm to rt. After 18 h at rt, the reaction was quenched with 1 N HCl (60 mL) and extracted with EtOAc (3×100 mL). The combined extracts were washed with brine (1×100 mL), dried (MgSO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (CH2Cl2→5% MeOH/CH2Cl2, gradient) afforded 3.2 g (35%) of (4-hydroxy-but-2-ynyloxy)-acetic acid methyl ester. After 18 h at rt the reaction was quenched with 1 N HCl (60 mL) extracted with EtOAc (3×100 mL) The combined extracts were washed with brine (1×100 mL) dried (MgSO4) filtered concentrated in vacuo Purification of the residue by flash column chromatography on silica gel (CH2Cl2→5% MeOH/CH2Cl2, gradient)
来源 ID: ord-ef0148b150e840c5a4174154adc19643PubChem References
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