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Phosphorus oxychloride → 4-Chloro-5-(4-methylphenyl)pyrimidine

HRID 274578
Notes
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Reaction equation

HRID 274578 reaction equation
O[C:2]1[C:7]([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=2)=[CH:6][N:5]=[CH:4][N:3]=1.P(Cl)(Cl)([Cl:17])=O>>[Cl:17][C:2]1[C:7]([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=2)=[CH:6][N:5]=[CH:4][N:3]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 178423875HCID 178423875, compound

Product 1

HCID 200930324-Chloro-5-(4-methylphenyl)pyrimidineYield 71%

Procedure

A mixture of 4-hydroxy-5-(p-tolyl)pyrimidine (9 g, 48 mmol) and phosphorous oxychloride (44 ml) was heated under reflux for 2 hours. After the reaction mixture was concentrated to dryness, the residue was poured into iced water to precipitate crystals which were extraced with methylene chloride. The extract was washed with water, dried and concentrated to dryness. The residue was purified by column chromatography on silica gel to afford colorless powders (7 g, 71%), m.p. 67°-70° C.

Workup

  1. temperaturewas heated
  2. temperatureunder reflux for 2 hours
  3. concentrationAfter the reaction mixture was concentrated to dryness
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
addition
the residue was poured into iced water
  • customto precipitate crystals which
  • washThe extract was washed with water
  • customdried
  • concentrationconcentrated to dryness
  • customThe residue was purified by column chromatography on silica gel
  • Sources & evidence

    ORD record
    ord-676a0fad813844709279e9a036027c45
    Source dataset
    uspto-grants-1995_02
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05389641

    Reaction notes

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