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

HRID 1245759
Notes
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Reaction equation

HRID 1245759 reaction equation
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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

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

Product 1

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

Procedure

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.

Workup

  1. temperaturewas heated
  2. temperatureat reflux for 1 hour
  • temperatureThe mixture was cooled
  • customevaporated to dryness
  • additionThe residue was poured into ice-water
  • extractionextracted with ethyl acetate
  • washThe organic layer was washed with brine
  • customdried
  • concentrationconcentrated to dryness
  • Sources & evidence

    ORD record
    ord-dd9ab086c0c94f9495963f2059dba634
    Source dataset
    uspto-grants-2006_10
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07125880B1

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes