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Phosphorus oxychloride → HCID 18327906、化合物

HRID 1250303
ノート
印刷プレビュー

反応式

HRID 1250303 の反応式
[C:1]([O:5][C:6]([N:8]1[CH:13]=[CH:12][C:11](O)([C:14]2[N:19]=[CH:18][CH:17]=[CH:16][N:15]=2)[CH:10]=[CH:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].P(Cl)(Cl)(Cl)=O>N1C=CC=CC=1>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][C:11]([C:14]2[N:15]=[CH:16][CH:17]=[CH:18][N:19]=2)=[CH:10][CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
参加物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 24813Phosphorus oxychlorideHCID 18328032HCID 18328032、化合物

生成物 1

HCID 18327906HCID 18327906、化合物収率 51%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

2.11 g of the compound of step 1 of Example 25 was dissolved in 30 ml of pyridine, then 1.0 ml (1.4 equivalents) of phosphorus oxychloride was added under ice cooling and the result was agitated for 15 hours. The pyridine was distilled off under reduced pressure, an aqueous solution of 10% sodium hydroxide was added and extraction was performed by methylene chloride. The organic layer was washed with saturated saline and was dried by anhydrous magnesium sulfate, then the solvent was distilled off and the resultant crude product was refined with silica gel column chromatography (hexane:ethyl acetate=2:1) to obtain the above-referenced compound in an amount of 1.01 g (yield of 51%).

後処理

  1. distillationThe pyridine was distilled off under reduced pressure
  2. additionan aqueous solution of 10% sodium hydroxide was added
  3. extractionextraction
  4. washThe organic layer was washed with saturated saline
  5. dry with materialwas dried by anhydrous magnesium sulfate
  6. distillationthe solvent was distilled off
  7. customto obtain the above-referenced compound in an amount of 1.01 g (yield of 51%)

出典と根拠

ORDレコード
ord-b6c8df10395e43e1be627324484d5cb5
出典データセット
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06337397B1

反応ノート

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