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Phosphorus oxychloride → 4-Chloro-2-ethylthieno(3,2-d)pyrimidine

HRID 478066
Notes
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Reaction equation

HRID 478066 reaction equation
[CH2:1]([C:3]1[N:4]=[C:5](O)[C:6]2[S:11][CH:10]=[CH:9][C:7]=2[N:8]=1)[CH3:2].P(Cl)(Cl)([Cl:15])=O>>[Cl:15][C:5]1[C:6]2[S:11][CH:10]=[CH:9][C:7]=2[N:8]=[C:3]([CH2:1][CH3:2])[N:4]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 178437764HCID 178437764, compound

Product 1

HCID 107031404-Chloro-2-ethylthieno(3,2-d)pyrimidine

Procedure

2-Ethyl-4-hydroxythieno[3,2-d]pyrimidine (0.6725 g, 0.00373M) was refluxed with phosphorus oxychloride (20 ml) for 2 hours. The reaction mixture was cooled, concentrated under vacuum, the residue dissolved in methylene chloride, poured over ice and water and basified with ammonia. The layers were separated and the aqueous layer extracted with ether. The combined organic extracts were washed with brine, dried (MgSO4) and concentrated under vacuum to obtain the product, 0.65 g, as a tan solid, m.p. 46°-48° C. the structure of which was confirmed by NMR.

Workup

  1. temperatureThe reaction mixture was cooled
  2. concentrationconcentrated under vacuum
  3. dissolutionthe residue dissolved in methylene chloride
  4. addition
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
poured over ice and water and basified with ammonia
  • customThe layers were separated
  • extractionthe aqueous layer extracted with ether
  • washThe combined organic extracts were washed with brine
  • dry with materialdried (MgSO4)
  • concentrationconcentrated under vacuum
  • customto obtain the product, 0.65 g
  • Sources & evidence

    ORD record
    ord-586c38cf10a64d378fa2584155ead93b
    Source dataset
    uspto-grants-1989_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04889856

    Reaction notes

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