反応 #4065465
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9467cc2e89774a9b9753f01fe117c64b表示可能な構造データがありません
CCC(CC)C(=O)OCC製品情報
ethyl 2-ethylbutanoate (CAS 2983-38-2) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 76326
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9467cc2e89774a9b9753f01fe117c64b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-304ccd07a9084b35a9d377dc1163069b反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-33350e08be0048d09bf54717a42189b2反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-33350e08be0048d09bf54717a42189b2反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-303828d9874944f69552c1a2e4c7233c反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-303828d9874944f69552c1a2e4c7233c反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-a5a538a6c7b34f7eb58104d1699de5d8反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-a5a538a6c7b34f7eb58104d1699de5d8反応条件: temp:-78.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-f48209b11f0e45e3b8354b1076b98e8e反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-33350e08be0048d09bf54717a42189b2反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-303828d9874944f69552c1a2e4c7233c反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-a5a538a6c7b34f7eb58104d1699de5d8PubChem References
化合物の公開データベース記録に掲載された情報源です。
