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HCID 19707490, compound → Methyl 3-(3-aminophenoxy)benzoate

HRID 726916
Notes
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Reaction equation

HRID 726916 reaction equation
[C:1]([C:5]1[CH:6]=[C:7]([O:11][C:12]2[CH:13]=[C:14]([N+:18]([O-])=O)[CH:15]=[CH:16][CH:17]=2)[CH:8]=[CH:9][CH:10]=1)([O:3][CH3:4])=[O:2]>CO.[Pd]>[C:1]([C:5]1[CH:6]=[C:7]([O:11][C:12]2[CH:13]=[C:14]([NH2:18])[CH:15]=[CH:16][CH:17]=2)[CH:8]=[CH:9][CH:10]=1)([O:3][CH3:4])=[O:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 19707490HCID 19707490, compound

Product 1

HCID 19707463Methyl 3-(3-aminophenoxy)benzoate

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 887MethanolSolvent

Procedure

To a solution of 1 (440 mg) in 30 mL of methanol under a nitrogen atmosphere was added 10% Pd/C (30 mg). The solution was purged with H2 gas, then stirred at room temperature under a balloon atmosphere of H2. After 8 h, the reaction was flushed with nitrogen and filtered through celite to remove the catalyst, then concentrated in vacuo. The resulting brown oil was used without further purification.

Workup

  1. customThe solution was purged with H2 gas
  2. customthe reaction was flushed with nitrogen
  3. filtrationfiltered through celite
  4. customto remove the catalyst
  5. concentrationconcentrated in vacuo
  6. customThe resulting brown oil was used without further purification

Sources & evidence

ORD record
ord-25f92af004524f0abfbf98156f624366
Source dataset
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05710171

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes