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Phosphorus oxychloride → 184913-07-3

HRID 1871456
Notes
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Reaction equation

HRID 1871456 reaction equation
[CH3:1][C:2]1[NH:7][C:6](=O)[C:5]2[CH:9]=[CH:10][S:11][C:4]=2[CH:3]=1.P(Cl)(Cl)([Cl:14])=O>>[Cl:14][C:6]1[C:5]2[CH:9]=[CH:10][S:11][C:4]=2[CH:3]=[C:2]([CH3:1])[N:7]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 18691205HCID 18691205, compound

Product 1

HCID 18691213184913-07-3

Procedure

A solution of 6.2 g of 6-methylthieno[3,2-c]pyridin-4(5H)-one in 30 ml of phosphoryl chloride was heated under reflux for 1 hour. After being cooled, the excess phosphoryl chloride was removed under reduced pressure, and the residue was poured into ice water, made basic with aqueous 2N sodium hydroxide and extracted with chloroform. The extract was washed successively with water and saturated saline, and dried over anhydrous magnesium sulfate. The drying agent was removed by filtration, and the solvent was removed under reduced pressure to give 7.0 g of 4-chloro-6-methylthieno[3,2-c]pyridine as a brown oily material.

Workup

  1. temperatureunder reflux for 1 hour
  2. temperatureAfter being cooled
  3. customthe excess phosphoryl chloride was removed under reduced pressure
  • additionthe residue was poured into ice water
  • extractionextracted with chloroform
  • washThe extract was washed successively with water and saturated saline
  • dry with materialdried over anhydrous magnesium sulfate
  • customThe drying agent was removed by filtration
  • customthe solvent was removed under reduced pressure
  • Sources & evidence

    ORD record
    ord-c3fc52c9b5b54040add3f3650f04e385
    Source dataset
    uspto-grants-2000_08
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US06103736

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes