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1,4-Dioxane → HCID 178479751, compound

HRID 1826909
Notes
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Reaction equation

HRID 1826909 reaction equation
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]3[O:14][CH2:13][O:12][C:9]=3[CH:10]=2)[N:5]=[CH:4][C:3]=1[C:15]([O:17]CC)=[O:16].[O:20]1CCOCC1>>[ClH:1].[OH:20][C:2]1[C:11]2[C:6](=[CH:7][C:8]3[O:14][CH2:13][O:12][C:9]=3[CH:10]=2)[N:5]=[CH:4][C:3]=1[C:15]([OH:17])=[O:16]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 312751,4-DioxaneHCID 8245791,3-Dioxolo(4,5-g)quinoline-7-carboxylic acid, 8-chloro-, ethyl ester

Product 1

HCID 178479751HCID 178479751, compound

Procedure

Ethyl 4-chloro-6,7-methylenedioxyquinoline-3-carboxylate (18.5 g, 66.2 mmol) was dissolved in dioxane (100 mL) and treated with 50 mL 5 NNaOH and heated at reflux for 2 hour. After this time the solution was concentrated on a rotary evaporator, cooled and extracted with dichloromethane (2×100 mL). The remaining aqueous solution was then acidified with concentrated HCl and the precipitate collected and dried to afford 7 g of crude 4-hydroxy-6,7-methylenedioxyquinoline-3-carboxylic acid hydrochloride.

Workup

  1. temperatureheated
  2. temperatureat reflux for 2 hour
  3. concentrationAfter this time the solution was concentrated on a rotary evaporator
  • temperaturecooled
  • extractionextracted with dichloromethane (2×100 mL)
  • customthe precipitate collected
  • customdried
  • Sources & evidence

    ORD record
    ord-8f7fa91b84384c239207573cd35e246f
    Source dataset
    uspto-grants-2006_05
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07053104B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes