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

HRID 1737700
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인쇄 미리보기

반응식

HRID 1737700 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 1784248682,5-dimethyl-6-[(2,4,6-trimethylphenyl)methyl]-1H-pyrimidin-4-one

생성물 1

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

실험 절차

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.

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 1 hour
  3. temperatureThe mixture was cooled
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
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
  • 출처 및 근거

    ORD 기록
    ord-260268c894bf48258a49c59ec5aea1d9
    출처 데이터셋
    uspto-grants-1999_10
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05962479

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