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Benzoic Acid → HCID 85109113, compound

HRID 1394163
Notes
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Reaction equation

HRID 1394163 reaction equation
[CH:1]([C:3]1[CH:4]=[C:5]([C:9]2[CH:14]=[CH:13][C:12]([O:15][C:16]([F:19])([F:18])[F:17])=[CH:11][CH:10]=2)[CH:6]=[CH:7][CH:8]=1)=O.[S:20]1[CH2:24][C:23](=[O:25])[NH:22][C:21]1=[O:26].N1CCCCC1.C(O)(=O)C1C=CC=CC=1>C1(C)C=CC=CC=1.O>[F:17][C:16]([F:19])([F:18])[O:15][C:12]1[CH:13]=[CH:14][C:9]([C:5]2[CH:4]=[C:3]([CH:8]=[CH:7][CH:6]=2)[CH:1]=[C:24]2[S:20][C:21](=[O:26])[NH:22][C:23]2=[O:25])=[CH:10][CH:11]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 243Benzoic AcidHCID 5437ThiazolidinedioneHCID 8082PiperidineHCID 27607194'-Trifluoromethoxy-biphenyl-3-carbaldehyde

Product 1

HCID 85109113HCID 85109113, compound

Reagents, catalysts & solvents 2

HCID 962WaterSolvent
HCID 1140TolueneSolvent

Procedure

To a solution of 3-formyl-(4′-trifluoromethoxy-1,1′-biphenyl) (0.31 g, 1.16 mmol) and 2,4-thiazolidinedione (0.164 g, 1.4 mmol) in toluene (20 mL) were added piperidine (0.015 mL, 0.152 mmol) and benzoic acid (0.021 mg, 0.175 mmol), and the reaction was refluxed for 3 h with continuous removal of water. The solvent was then distilled off and the residue was crystallized from ether-pet ether to yield titled product as a solid.

Workup

  1. distillationThe solvent was then distilled off
  2. customthe residue was crystallized from ether-pet ether

Sources & evidence

ORD record
ord-6726ee244e344d4fbf2cd3b57d98d87a
Source dataset
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07348348B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes