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Dimethyl 2-(4'-methoxy-3-nitrobiphenyl-4-yl)malonate → 4'-Methoxy-3-nitrobiphenyl-4-acetic acid

HRID 428277
Notes
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Reaction equation

HRID 428277 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][C:12]([CH:15](C(OC)=O)[C:16]([O:18]C)=[O:17])=[C:11]([N+:24]([O-:26])=[O:25])[CH:10]=2)=[CH:5][CH:4]=1>Cl>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:9]2[CH:14]=[CH:13][C:12]([CH2:15][C:16]([OH:18])=[O:17])=[C:11]([N+:24]([O-:26])=[O:25])[CH:10]=2)=[CH:7][CH:8]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 10737157Dimethyl 2-(4'-methoxy-3-nitrobiphenyl-4-yl)malonate

Product 1

HCID 104935034'-Methoxy-3-nitrobiphenyl-4-acetic acid

Reagents, catalysts & solvents 1

HCID 313Hydrochloric AcidSolvent

Procedure

Crude dimethyl 4′-methoxy-3-nitro-biphenyl-4-malonate was heated at 100° C. in 60 mL of 6N hydrochloric acid for 15 hours and cooled. The precipitate was collected by filtration, washed with water and hexane, arid dried to give 7.2 g of crude 4′-methoxy-3-nitrobiphenyl-4-acetic acid as a light tan solid.

Workup

  1. temperaturecooled
  2. filtrationThe precipitate was collected by filtration
  3. wash
washed with water and hexane
  • customarid dried
  • Sources & evidence

    ORD record
    ord-174078e1a08f454b848b988f61c931bc
    Source dataset
    uspto-grants-2001_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US06313158B1

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes