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Phosphorus oxychloride → 4-Chloro-2,5-dimethyl-6-(2,4,6-trimethyl-benzyl)pyrimidine

HRID 968030
ノート
印刷プレビュー

反応式

HRID 968030 の反応式
O[C:2]1[C:7]([CH3:8])=[C:6]([CH2:9][C:10]2[C:15]([CH3:16])=[CH:14][C:13]([CH3:17])=[CH:12][C:11]=2[CH3:18])[N:5]=[C:4]([CH3:19])[N:3]=1.O=P(Cl)(Cl)[Cl:22]>>[Cl:22][C:2]1[C:7]([CH3:8])=[C:6]([CH2:9][C:10]2[C:15]([CH3:16])=[CH:14][C:13]([CH3:17])=[CH:12][C:11]=2[CH3:18])[N:5]=[C:4]([CH3:19])[N:3]=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 1784248682,5-dimethyl-6-[(2,4,6-trimethylphenyl)methyl]-1H-pyrimidin-4-one

生成物 1

HCID 219124244-Chloro-2,5-dimethyl-6-(2,4,6-trimethyl-benzyl)pyrimidine収率 97%

実験手順

A mixture of 4-hydroxy-2,5-dimethyl-6-(2,4,6-trimethyl-benzyl)-pyrimidine (1.2 g, 4.68 mmol) and POCl3 (25 ml) was heated at reflux for 1 hour. The mixture was cooled and evaporated to dryness. The residue was poured into ice-water and extracted with ethyl acetate. The organic layer was washed with brine, dried and concentrated to dryness to give 1.24 g (97%) of golden crystals, mp 82-84° C.

後処理

  1. temperaturewas heated
  2. temperatureat reflux for 1 hour
  3. temperatureThe mixture was cooled
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
custom
evaporated to dryness
  • additionThe residue was poured into ice-water
  • extractionextracted with ethyl acetate
  • washThe organic layer was washed with brine
  • customdried
  • concentrationconcentrated to dryness
  • 出典と根拠

    ORDレコード
    ord-478286174ac8407cac560570d8455b1e
    出典データセット
    uspto-grants-2005_10
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US06956047B1

    反応ノート

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