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Phosphorus oxychloride → HCID 57860520、化合物

HRID 1947112
ノート
印刷プレビュー

反応式

HRID 1947112 の反応式
O[C:2]1[C:11]2[CH2:10][CH2:9][CH2:8][CH2:7][C:6]=2[NH:5][C:4](=[O:12])[C:3]=1[C:13]([O:15][CH2:16][CH3:17])=[O:14].P(Cl)(Cl)([Cl:20])=O>>[Cl:20][C:2]1[C:11]2[CH2:10][CH2:9][CH2:8][CH2:7][C:6]=2[NH:5][C:4](=[O:12])[C:3]=1[C:13]([O:15][CH2:16][CH3:17])=[O:14]
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

3

反応物 2

HCID 24813Phosphorus oxychlorideHCID 54682948HCID 54682948、化合物

生成物 1

HCID 57860520HCID 57860520、化合物収率 17%

反応条件

温度
130 °C

実験手順

A mixture of ethyl 4-hydroxy-2-oxo-1,2,5,6,7,8-hexahydroquinoline-3-carboxylate (26.0 g, 110 mmol) and phosphorus oxychloride (51.3 mL) was stirred at 130° C. for 1.5 hr. After cooling, the reaction mixture was concentrated under reduced pressure, and ice was added to the residue. The mixture was neutralized with saturated sodium hydrogen carbonate solution, and extracted with ethyl acetate. The extract was washed successively with saturated sodium hydrogen carbonate solution, water and brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was collected by filtration, and washed with ethyl acetate-hexane to give the title compound (4.65 g, 17%) as a white solid.

後処理

  1. temperatureAfter cooling
  2. concentrationthe reaction mixture was concentrated under reduced pressure, and ice
  3. additionwas added to the residue
  4. extractionextracted with ethyl acetate
  5. washThe extract was washed successively with saturated sodium hydrogen carbonate solution, water and brine
  6. dry with materialdried over magnesium sulfate
  7. concentrationconcentrated under reduced pressure
  8. filtrationThe residue was collected by filtration
  9. washwashed with ethyl acetate-hexane

出典と根拠

ORDレコード
ord-07248125c2164fb5937bfc0e0da907d4
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08399449B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート