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Methyl iodide → Methyl 3-cyclopropyl-2-methyl-3-oxopropanoate

HRID 498889
ノート
印刷プレビュー

反応式

HRID 498889 の反応式
CI.COC(=O)CC(=O)C1CC1>O=C([O-])[O-].[K+].[K+]>COC(=O)C(C)C(=O)C1CC1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6328Methyl iodideHCID 101300163-Cyclopropyl-3-Oxopropionic Acid Methyl Ester

生成物 1

HCID 61685373Methyl 3-cyclopropyl-2-methyl-3-oxopropanoate収率 79%

試薬・触媒・溶媒 1

HCID 11430Potassium Carbonate試薬

反応条件

温度
25 °C

実験手順

To a 500 ml round bottomed flask equipped with a magnetic stir bar under N2 atmosphere was charged methyl 3-cyclopropyl-3-oxopropanoate 1 (39.2 g, 276 mmol), MeI (17.2 ml, 276 mmol) and K2CO3 (57.2 g, 414 mmol). The mixture was agitated at 25 °C for 16 h. The reaction mixture was diluted with Et2O (100 ml) and filtered. The solids were rinsed with Et2O (100 ml) and the filtrate was concentrated to a crude oil. The crude oil was purified by normal phase column chromatography to give methyl 3-cyclopropyl-2-methyl-3-oxopropanoate 2 in 79% yield.

後処理

  1. additionThe reaction mixture was diluted with Et2O (100 mL).
  2. filtrationfiltrate 相を保持
  3. washThe solids were rinsed with Et2O (100 mL).
  4. concentrationThe filtrate was concentrated to a crude oil.
  5. other chromatographyThe crude oil was purified by normal phase column chromatography.

出典と根拠

ORDレコード
ord-8b0645e6b72740d2a995676b85386226
出典データセット
Development of an automated kinetic profiling system with online HPLC for reaction optimization
DOI
10.1039/c9re00086k
元リンク
出典を表示

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