反应 #4065465
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-9467cc2e89774a9b9753f01fe117c64b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-9467cc2e89774a9b9753f01fe117c64b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-304ccd07a9084b35a9d377dc1163069b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Using ethyl 2-ethylbutyrate and 1,4-dibromobutane, the same reaction as in Reference Example 16 was conducted to produce the title compound. b.p. 125°-130° C./0.3 mmHg the same reaction as in Reference Example 16
来源 ID: ord-33350e08be0048d09bf54717a42189b2反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Using ethyl 2-ethylbutyrate and 1,4-dibromobutane, the same reaction as in Reference Example 16 was conducted to produce the title compound. b.p. 125°-130° C./0.3 mmHg the same reaction as in Reference Example 16
来源 ID: ord-33350e08be0048d09bf54717a42189b2反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Using ethyl 2-ethylbutyrate and 1,3-dibromopropane, the same reaction as in Reference Example 16 was conducted to produce the title compound. b.p. 98°-102° C./0.3 mmHg the same reaction as in Reference Example 16
来源 ID: ord-303828d9874944f69552c1a2e4c7233c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Using ethyl 2-ethylbutyrate and 1,3-dibromopropane, the same reaction as in Reference Example 16 was conducted to produce the title compound. b.p. 98°-102° C./0.3 mmHg the same reaction as in Reference Example 16
来源 ID: ord-303828d9874944f69552c1a2e4c7233c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Using ethyl 2-ethylbutyrate and 1-bromo-2-chloroethane, the same reaction as in Reference Example 16 was conducted to produce the title compound. b.p. 69°-72° C./0.3 mmHg the same reaction as in Reference Example 16
来源 ID: ord-a5a538a6c7b34f7eb58104d1699de5d8反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Using ethyl 2-ethylbutyrate and 1-bromo-2-chloroethane, the same reaction as in Reference Example 16 was conducted to produce the title compound. b.p. 69°-72° C./0.3 mmHg the same reaction as in Reference Example 16
来源 ID: ord-a5a538a6c7b34f7eb58104d1699de5d8反应条件: temp:-78.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of ethyl 2-ethylbutyrate (21.60 g, 150 mmol) in THF (25 mL) was added dropwise to a solution of lithium diisopropylamide prepared by treating diisopropylamine (16.67 g, 165 mmol) in dry THF (150 mL) with butyllithium in hexanes (2.5M, 66 mL, 165 mmol) at -78° C. for 1 h in a nitrogen atmosphere. The resulting mixture was stirred at -78° C. for 1 h, then a solution of bromoacetonitrile (21.60 g, 180 mmol) in THF (50 mL) was introduced slowly over a period of 30 minutes (the reaction mixture starts getting darker as the addition progresses). The resulting dark mixture was stirred overnight (ca. 16 h) and allowed to warm from -78° C. to room temperature. The reaction was quenched by addition of HCl (1 N, 250 mL) at 0° C. The layers were separated, and the aqueous phase was further extracted with ether (3×100 mL). The combined organic extract was washed sequentially with 75 mL portions of saturated NaHCO3, water (several times), and brine, and dried over MgSO4. The solvent was removed in vacuo to give 27.77 g of dark colored liquid. After two vacuum distillations, the nitrile (12.35 g, 45%) was obtained as a colorless liquid: bp 84-85° C. (1.3 mmHg). Analytical sample was prepared by column chromatography over silica gel (hexanes-EtOAc, 19:1) followed by bulb-to-bulb distillation (pot temp. 80° C. (1 mmHg)). prepared starts getting darker as the addition progresses) The resulting dark mixture was stirred overnight (ca. 16 h) to warm from -78° C. to room temperature The reaction was quenched by addition of HCl (1 N, 250 mL) at 0° C The layers were separated the aqueous phase was further extracted with ether (3×100 mL) The combined organic extract was washed sequentially with 75 mL portions of saturated NaHCO3, water (several times), and brine dried over MgSO4 The solvent was removed in vacuo
来源 ID: ord-f48209b11f0e45e3b8354b1076b98e8e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Using ethyl 2-ethylbutyrate and 1,4-dibromobutane, the same reaction as in Reference Example 16 was conducted to produce the title compound. b.p. 125°-130° C./0.3 mmHg the same reaction as in Reference Example 16
来源 ID: ord-33350e08be0048d09bf54717a42189b2反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Using ethyl 2-ethylbutyrate and 1,3-dibromopropane, the same reaction as in Reference Example 16 was conducted to produce the title compound. b.p. 98°-102° C./0.3 mmHg the same reaction as in Reference Example 16
来源 ID: ord-303828d9874944f69552c1a2e4c7233c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Using ethyl 2-ethylbutyrate and 1-bromo-2-chloroethane, the same reaction as in Reference Example 16 was conducted to produce the title compound. b.p. 69°-72° C./0.3 mmHg the same reaction as in Reference Example 16
来源 ID: ord-a5a538a6c7b34f7eb58104d1699de5d8PubChem References
以下资料来自该化合物的公开数据库参考记录。
