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Phosphorus oxychloride → 4-Chloro-2-methoxy-6-methylpyrimidine

HRID 1193395
Notes
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Reaction equation

HRID 1193395 reaction equation
[CH3:1][O:2][C:3]1[NH:8][C:7](=O)[CH:6]=[C:5]([CH3:10])[N:4]=1.O=P(Cl)(Cl)[Cl:13]>>[Cl:13][C:7]1[CH:6]=[C:5]([CH3:10])[N:4]=[C:3]([O:2][CH3:1])[N:8]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 1354372732-Methoxy-6-methyl-3,4-dihydropyrimidin-4-one

Product 1

HCID 134258364-Chloro-2-methoxy-6-methylpyrimidineYield 2.3%

Procedure

2-Methoxy-6-methylpyrimidin-4(3H)-one (12 g, 85.71 mmol, 1 eq) was heated for 30-40 min at 100° C. in POCl3 (85 ml). The reaction mixture was then concentrated and diluted with ice-water (100 ml). The aqueous phase was rendered alkaline (pH˜9) with NaHCO3 and extracted with ethyl acetate (2×200 ml). The combined organic phases were washed with saturated sodium chloride solution (100 ml), dried over sodium sulfate and concentrated under reduced pressure. The crude product was purified by column chromatography (silica gel, 2% ethyl acetate/hexane). The desired product was in the form of a light-yellow solid. Yield: 2.3% (300 mg, 1.8987 mmol) after 2 stages

Workup

concentration
The reaction mixture was then concentrated
  • additiondiluted with ice-water (100 ml)
  • extractionextracted with ethyl acetate (2×200 ml)
  • washThe combined organic phases were washed with saturated sodium chloride solution (100 ml)
  • dry with materialdried over sodium sulfate
  • concentrationconcentrated under reduced pressure
  • customThe crude product was purified by column chromatography (silica gel, 2% ethyl acetate/hexane)
  • Sources & evidence

    ORD record
    ord-09c393e80844477ab0b28ad593b8cb2b
    Source dataset
    uspto-grants-2014_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08680159B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes