反应 #4132014
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-5e51c7975bc34a5085cde80049ffa2d7暂无可渲染的结构数据
CCOC(=O)C=C1CCC1产品信息
2-环丁烯乙酸乙酯(CAS 27741-65-7)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
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5e51c7975bc34a5085cde80049ffa2d7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5622b48d92334f3e8b38291643dcbcdd反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-33e19d521f7449839b4f91c15edc05c0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2bdeb80b77ab4408a7cc8a4504342563反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The unsaturated ester (2) (5.79 g, 41.4 mmol) was dissolved in tetrahydrofuran (20 mL) and stirred at 70° C. with nitromethane (4.67 mL, 86.4 mmol) and tetrabutylammonium fluoride (1.0 M in tetrahydrofuran, 55 mL, 55.0 mmol). After 18 hours, the mixture was cooled to room temperature, diluted with ethyl acetate (150 mL), and washed with 2N HCl (60 mL) followed by brine (100 mL). The organic phase was collected, dried (MgSO4), and the solvent removed in vacuo. The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1) to give 4.34 g (52%) of a clear oil. washed with 2N HCl (60 mL) The organic phase was collected dried (MgSO4) the solvent removed in vacuo The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1)
来源 ID: ord-018f0f0cbc414716bc95ff1046ea1805反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The unsaturated ester (2) (5.79 g, 41.4 mmol) was dissolved in tetrahydrofuran (20 mL) and stirred at 70° C. with nitromethane (4.67 mL, 86.4 mmol) and tetrabutylammonium fluoride (1.0 M in tetrahydrofuran, 55 mL, 55.0 mmol). After 18 hours, the mixture was cooled to room temperature, diluted with ethyl acetate (150 mL), and washed with 2N HCl (60 mL) followed by brine (100 mL). The organic phase was collected, dried (MgSO4), and the solvent removed in vacuo. The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1) to give 4.34 g (52%) of a clear oil. washed with 2N HCl (60 mL) The organic phase was collected dried (MgSO4) the solvent removed in vacuo The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1)
来源 ID: ord-018f0f0cbc414716bc95ff1046ea1805反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The unsaturated ester (2) (5.79 g, 41.4 mmol) was dissolved in tetrahydrofuran (20 mL) and stirred at 70° C. with nitromethane (4.67 mL, 86.4 mmol) and tetrabutylammonium fluoride (1.0 M in tetrahydrofuran, 55 mL, 55.0 mmol). After 18 hours, the mixture was cooled to room temperature, diluted with ethyl acetate (150 mL), and washed with 2N HCl (60 mL) followed by brine (100 mL). The organic phase was collected, dried (MgSO4), and the solvent removed in vacuo. The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1) to give 4.34 g (52%) of a clear oil. washed with 2N HCl (60 mL) The organic phase was collected dried (MgSO4) the solvent removed in vacuo The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1)
来源 ID: ord-df629faf40af426fab363e568fffe13a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The unsaturated ester (2) (5.79 g, 41.4 mmol) was dissolved in tetrahydrofuran (20 mL) and stirred at 70° C. with nitromethane (4.67 mL, 86.4 mmol) and tetrabutylammonium fluoride (1.0 M in tetrahydrofuran, 55 mL, 55.0 mmol). After 18 hours, the mixture was cooled to room temperature, diluted with ethyl acetate (150 mL), and washed with 2N HCl (60 mL) followed by brine (100 mL). The organic phase was collected, dried (MgSO4), and the solvent removed in vacuo. The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1) to give 4.34 g (52%) of a clear oil. washed with 2N HCl (60 mL) The organic phase was collected dried (MgSO4) the solvent removed in vacuo The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1)
来源 ID: ord-df629faf40af426fab363e568fffe13a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5e51c7975bc34a5085cde80049ffa2d7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5622b48d92334f3e8b38291643dcbcdd反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-33e19d521f7449839b4f91c15edc05c0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2bdeb80b77ab4408a7cc8a4504342563PubChem 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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