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Phosphorus oxychloride → 4-Chloro-5-nitropyrimidine

HRID 1044156
ノート
印刷プレビュー

反応式

HRID 1044156 の反応式
[N+:1]([C:4]1[C:5](O)=[N:6][CH:7]=[N:8][CH:9]=1)([O-:3])=[O:2].P(Cl)(Cl)([Cl:13])=O>C(#N)C.C(OCC)(=O)C>[Cl:13][C:5]1[C:4]([N+:1]([O-:3])=[O:2])=[CH:9][N:8]=[CH:7][N:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 24813Phosphorus oxychlorideHCID 178526815HCID 178526815、化合物

生成物 1

HCID 249037774-Chloro-5-nitropyrimidine収率 33%

試薬・触媒・溶媒 2

HCID 6342Acetonitrile溶媒HCID 8857Ethyl Acetate溶媒2 回

実験手順

The mixture of 5-nitropyrimidin-4-ol (1.04 g) and phosphorus oxychloride (5.66 g) in acetonitrile (10 mL) was stirred at reflux for 2 h. After this time, the reaction mixture was cooled to ambient temperature, diluted with ethyl acetate (50 mL), and filtered and the filtrate was concentrated under reduced pressure. The residue obtained was diluted with ethyl acetate (100 mL), washed with saturated aqueous sodium bicarbonate (50 mL) then brine (50 mL), and filtered and the filtrate was concentrated under reduced pressure. The residue obtained was purified by chromatography (silica, heptane to 1:3 ethyl acetate/heptane) to afford 4-chloro-5-nitropyrimidine (383 mg, 33%) as a colorless oil.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperatureat reflux for 2 h
  2. filtrationfiltered
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. customThe residue obtained
  5. washwashed with saturated aqueous sodium bicarbonate (50 mL)
  6. filtrationbrine (50 mL), and filtered
  7. concentrationthe filtrate was concentrated under reduced pressure
  8. customThe residue obtained
  9. customwas purified by chromatography (silica, heptane to 1:3 ethyl acetate/heptane)

出典と根拠

ORDレコード
ord-16efcbf33689479398115caa60bce83c
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08563575B2

反応ノート

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