反应 #4164427
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-1ea279d2c8d94e32853d193a4bd3b625暂无可渲染的结构数据
CCOC(=O)C1CC(CN1)O产品信息
乙基 4-羟基吡咯烷-2-羧酸乙酯(CAS 1079350-28-9)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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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1ea279d2c8d94e32853d193a4bd3b625反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0b9fbabbf72f448bb78e40f8c7e55ca9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1702f4521546472d9de9b1c42b5046ab反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6d0346860c5b4faaac64e08ef7424db4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d34e497cb1bf4636adaebf5868be2330反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-72d517b33a2b44d68990a8d2edb02c18反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1ea279d2c8d94e32853d193a4bd3b625反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-Fluoronitrobenzene (0.28 mL, 2.65 mmol), 4-hydroxy-pyrrolidine-2-carboxylic acid ethyl ester (419 mg, 2.65 mmol), and sodium bicarbonate (222 mg, 2.65 mmol) were dissolved in 5 mL dry DMF and heated to 80° C. After 24 h at this temperature, the reaction was cooled and water and ethyl acetate were added. The organic phase washed with brine, dried (MgSO4), and concentrated. Flash chromatography (65-75% ethyl acetate/hexanes) gave 260 mg (35% yield) of the desired product. 1H NMR (CDCl3, 500 MHz) 8.15 (d, J=9.3 Hz, 2H), 6.54 (d, J=9.3 Hz, 2H), 4.60 (m, 1H), 4.41 (d, J=9.2 Hz, 1H), 4.31 (dq, J=10.8, 7.1 Hz, 1H), 4.29 (dq, J=10.8, 7.1 Hz, 1H), 3.73 (dt, J=11.0, 1.2 Hz, 1H), 3.70 (dd, J=11.0, 4.2 Hz, 1H), 2.51 (ddd, J=14.2, 9.2, 4.2 Hz, 1H), 2.35 (dd, J=14.2, 1.2 Hz, 1H), 1.34 (t, J=7.1 Hz, 3H). the reaction was cooled The organic phase washed with brine dried (MgSO4) concentrated
来源 ID: ord-9828116ef54a41858e9aeeeac945cb3a反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-Fluoronitrobenzene (0.28 mL, 2.65 mmol), 4-hydroxy-pyrrolidine-2-carboxylic acid ethyl ester (419 mg, 2.65 mmol), and sodium bicarbonate (222 mg, 2.65 mmol) were dissolved in 5 mL dry DMF and heated to 80° C. After 24 h at this temperature, the reaction was cooled and water and ethyl acetate were added. The organic phase washed with brine, dried (MgSO4), and concentrated. Flash chromatography (65-75% ethyl acetate/hexanes) gave 260 mg (35% yield) of the desired product. 1H NMR (CDCl3, 500 MHz) 8.15 (d, J=9.3 Hz, 2H), 6.54 (d, J=9.3 Hz, 2H), 4.60 (m, 1H), 4.41 (d, J=9.2 Hz, 1H), 4.31 (dq, J=10.8, 7.1 Hz, 1H), 4.29 (dq, J=10.8, 7.1 Hz, 1H), 3.73 (dt, J=11.0, 1.2 Hz, 1H), 3.70 (dd, J=11.0, 4.2 Hz, 1H), 2.51 (ddd, J=14.2, 9.2, 4.2 Hz, 1H), 2.35 (dd, J=14.2, 1.2 Hz, 1H), 1.34 (t, J=7.1 Hz, 3H). the reaction was cooled The organic phase washed with brine dried (MgSO4) concentrated
来源 ID: ord-9828116ef54a41858e9aeeeac945cb3a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0b9fbabbf72f448bb78e40f8c7e55ca9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d34e497cb1bf4636adaebf5868be2330反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-72d517b33a2b44d68990a8d2edb02c18PubChem 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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