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Phosphorus oxychloride → 4-Chloro-2-methylthio-6-(3-trifluoromethyl-phenyl)-pyrimidine

HRID 2053086
ノート
印刷プレビュー

反応式

HRID 2053086 の反応式
[CH3:1][S:2][C:3]1[N:8]=[C:7](O)[CH:6]=[C:5]([C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([C:16]([F:19])([F:18])[F:17])[CH:11]=2)[N:4]=1.P(Cl)(Cl)([Cl:22])=O>>[Cl:22][C:7]1[CH:6]=[C:5]([C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([C:16]([F:19])([F:18])[F:17])[CH:11]=2)[N:4]=[C:3]([S:2][CH3:1])[N:8]=1
参加物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 1785035332-methylsulfanyl-6-[3-(trifluoromethyl)phenyl]-1H-pyrimidin-4-one

生成物 1

HCID 866125004-Chloro-2-methylthio-6-(3-trifluoromethyl-phenyl)-pyrimidine

実験手順

2-Methylsulfanyl-6-(3-trifluoromethyl-phenyl)-pyrimidin-4-ol (500 mg) and phosphorous oxychloride (2.5 ml) were heated to reflux for four hours. The reaction mixture was concentrated under reduced pressure and the remaining residue dissolved in ethyl acetate (50 ml) and washed with water (2×30 ml). Organics were separated, dried over sodium sulphate and solvent was removed under reduced pressure to yield 4-chloro-2-methylsulfanyl-6-(3-trifluoromethyl-phenyl)-pyrimidine (478 mg) as a brown solid.

後処理

  1. temperatureto reflux for four hours
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  • dissolutionthe remaining residue dissolved in ethyl acetate (50 ml)
  • washwashed with water (2×30 ml)
  • customOrganics were separated
  • dry with materialdried over sodium sulphate and solvent
  • customwas removed under reduced pressure
  • 出典と根拠

    ORDレコード
    ord-74c261d3192a46d1940be3c02b122c40
    出典データセット
    uspto-grants-2008_02
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07326715B2

    反応ノート

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