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Phosphorus oxychloride → HCID 58046417, compound

HRID 2046387
Notes
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Reaction equation

HRID 2046387 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[N:12][NH:11][C:10](=O)[CH:9]=2)=[CH:4][CH:3]=1.O=P(Cl)(Cl)[Cl:17]>>[Cl:17][C:10]1[N:11]=[N:12][CH:13]=[C:8]([C:5]2[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=2)[CH:9]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 67122910HCID 67122910, compound

Product 1

HCID 58046417HCID 58046417, compound

Conditions

Temperature
110 °C

Procedure

5-(4-Fluorophenyl)pyridazin-3(2H)-one (2.15 g, 11.3 mmol) was dissolved in POCl3 (133 ml) and the mixture was refluxed at 110° C. for 30 min. The reaction was cooled in an ice bath and slowly quenched with aqueous sodium hydrogen carbonate (200 mL). The mixture was extracted with ethyl acetate (3×200 mL). The combined organics were washed with water and brine, dried over anhydrous MgSO4, filtered, and concentrated under reduced pressure to afford the title compound. 1H NMR (500 MHz, CD3SOCD3) δ 9.67 (d, 1H); 8.28 (d, 1H); 8.07 (dd, 2H); 7.42 (t, 2H).

Workup

temperature
The reaction was cooled in an ice bath
  • customslowly quenched with aqueous sodium hydrogen carbonate (200 mL)
  • extractionThe mixture was extracted with ethyl acetate (3×200 mL)
  • washThe combined organics were washed with water and brine
  • dry with materialdried over anhydrous MgSO4
  • filtrationfiltered
  • concentrationconcentrated under reduced pressure
  • Sources & evidence

    ORD record
    ord-8daf62f8d478467ebe338f7601c3417d
    Source dataset
    uspto-grants-2013_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08592425B2

    Reaction notes

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    On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes