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Phosphorus oxychloride → 4,6-Dichloro-3-nitroquinoline

HRID 1672351
Notes
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Reaction equation

HRID 1672351 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][C:6]([N+:12]([O-:14])=[O:13])=[C:5]2O.O=P(Cl)(Cl)[Cl:18]>>[Cl:18][C:5]1[C:4]2[C:9](=[CH:10][CH:11]=[C:2]([Cl:1])[CH:3]=2)[N:8]=[CH:7][C:6]=1[N+:12]([O-:14])=[O:13]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 178526764HCID 178526764, compound

Product 1

HCID 106816704,6-Dichloro-3-nitroquinoline

Procedure

11 g (48.97 mmol) of 6-chloro-3-nitro-quinolin-4-ol (step b) in 80 ml of POCl3 are heated under reflux for 5 h (tlc-control). The cool reaction mixture is poured slowly into 1.5 l of ice water. The title compound separates as a solid. The mixture is stirred for 15 min, the temperature not exceeding 0-5° C. The solid is filtered off, washed with water and dissolved in 200 ml ethylacetate. The organic phase is washed with a mixture of 200 ml of water and 38 ml of a 2 N sodium hydroxide solution, then again with water. After drying over MgSO4, the solvent is evaporated almost to dryness; hexane is added to the residue and the title compound is isolated by filtration as a dark-grey powder. This material is used in the next step without further purification.

Workup

  1. temperatureunder reflux for 5 h (tlc-control)
  • customThe cool reaction mixture
  • Sources & evidence

    ORD record
    ord-67888815a2404f6ba6b4d1d6caf92105
    Source dataset
    uspto-grants-2011_08
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07998972B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes