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Hydrochloric Acid → HCID 15578422, compound

HRID 544177
Notes
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Reaction equation

HRID 544177 reaction equation
[C:1]1([C:11](=[O:23])[CH2:12][C:13](=[O:22])[CH2:14][C:15](=O)[C:16]([O:18]CC)=[O:17])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.Cl>O1CCOCC1>[C:1]1([C:11]2[O:23][C:15]([C:16]([OH:18])=[O:17])=[CH:14][C:13](=[O:22])[CH:12]=2)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 20447156HCID 20447156, compound

Product 1

HCID 15578422HCID 15578422, compound

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

This crude ester was dissolved in dioxan (50 ml) and concentrated hydrochloric acid (50 ml), and the solution was heated under reflux for 11/2 hours then concentrated under vacuum to give a brown solid. The solid was recrystallised from ethanol and from ethanol-water to give the title product (mp 248°-249° C. with decomposition).

Workup

  1. temperature
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
under reflux for 11/2 hours
  • concentrationthen concentrated under vacuum
  • customto give a brown solid
  • customThe solid was recrystallised from ethanol and from ethanol-water
  • Sources & evidence

    ORD record
    ord-833c8728a3f04f448557f52cb3dc7c54
    Source dataset
    uspto-grants-1984_05
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04448787

    Reaction notes

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