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Phosphorus oxychloride → HCID 13713228, compound

HRID 745941
Notes
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Reaction equation

HRID 745941 reaction equation
O[C:2]1[C:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[CH:6][N:5]=[C:4]2[CH2:13][CH2:14][CH2:15][C:3]=12.P(Cl)(Cl)([Cl:18])=O>>[Cl:18][C:2]1[C:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[CH:6][N:5]=[C:4]2[CH2:13][CH2:14][CH2:15][C:3]=12
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 178469462HCID 178469462, compound

Product 1

HCID 13713228HCID 13713228, compound

Procedure

A mixture of 2.6 g of ethyl 6,7-dihydro-4-hydroxy-5H-cyclopenta[b]pyridine-3-carboxylate [J. Heterocyclic Chem. 12, 1245 (1975)] and 100 mL of phosphorous oxychloride is refluxed for 2.5 hours. The excess phosphorous oxychloride is then removed by evaporating under reduced pressure. The residue is dissolved in chloroform and washed with ice-cold saturated sodium bicarbonate aqueous solution. The chloroform layer is separated, dried over magnesium sulfate, passed through a short silica gel column and evaporated to dryness to yield ethyl 4-chloro-6,7-dihydro-5H-cyclopenta[b]pyridine-3-carboxylate.

Workup

  1. temperatureis refluxed for 2.5 hours
  2. customThe excess phosphorous oxychloride is then removed
  3. customby evaporating under reduced pressure
  • dissolutionThe residue is dissolved in chloroform
  • washwashed with ice-cold saturated sodium bicarbonate aqueous solution
  • customThe chloroform layer is separated
  • dry with materialdried over magnesium sulfate
  • customevaporated to dryness
  • Sources & evidence

    ORD record
    ord-4aa7d050aab243e6924c3fa4561faf16
    Source dataset
    uspto-grants-1986_07
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04602014

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes