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Sodium Iodide → Ethyl 3-Hydroxybutyrate

HRID 327865
ノート
印刷プレビュー

反応式

HRID 327865 の反応式
[Na+].[I-].[C:3]([O:9][CH2:10][CH3:11])(=[O:8])[CH2:4][C:5]([CH3:7])=[O:6].[H][H]>O>[OH:6][CH:5]([CH3:7])[CH2:4][C:3]([O:9][CH2:10][CH3:11])=[O:8]
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

5

反応物 3

HCID 5238Sodium IodideHCID 8868Ethyl AcetoacetateHCID 178418361HCID 178418361、化合物3 回

生成物 1

HCID 62572Ethyl 3-Hydroxybutyrate収率 63%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
65 °C

実験手順

Under a nitrogen gas atmosphere, 0.0096 g (7.3×10-6 mol) of [RuI(p-Cymene)((+)-SO3Na-BINAP)]I, 0.1164 g (7.8×10-4 mol) of NaI, 1 ml (7.5×10-3 mol) of ethyl acetoacetate, and 1.5 ml of water were charged in a 100 milli-liter autoclave. After displacing the inside atmosphere of the autoclave with a hydrogen gas, the autoclave was pressed at a hydrogen pressure of 50 kg/cm2 and the mixture was stirred for 40 hours at 65° C. After the reaction was over, the hydrogen gas was removed, and after added thereto 100 ml of water and 100 ml of ether, the ether extraction was carried out. The ether extract was recovered, dried with anhydrous sodium sulfate, and further ether was distilled off to provide 0.62 g (percent yield 63%) of ethyl 3-hydroxybutyrate. By the analysis of gas chromatography (PEG-HT), the conversion ratio was determined to be 99%.

後処理

  1. customwas removed
  2. additionafter added
  3. extraction100 ml of water and 100 ml of ether, the ether extraction
  4. extractionThe ether extract
  5. customwas recovered
  6. dry with materialdried with anhydrous sodium sulfate, and further ether
  7. distillationwas distilled off

出典と根拠

ORDレコード
ord-5ab3e6632dd54e23a7176b1dc9864c6e
出典データセット
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05274146

反応ノート

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