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HCID 66965255, compound → HCID 66965766, compound

HRID 1514973
Notes
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Reaction equation

HRID 1514973 reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]([NH:9][C:10](=[O:21])[C:11]2[CH:16]=[CH:15][C:14]([OH:17])=[C:13]([N+:18]([O-])=O)[CH:12]=2)[CH:5]=[CH:6][C:7]=1[CH3:8]>C(O)C.O=[Pt]=O>[NH2:18][C:13]1[CH:12]=[C:11]([CH:16]=[CH:15][C:14]=1[OH:17])[C:10]([NH:9][C:4]1[CH:5]=[CH:6][C:7]([CH3:8])=[C:2]([CH3:1])[CH:3]=1)=[O:21]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 66965255HCID 66965255, compound

Product 1

HCID 66965766HCID 66965766, compound

Reagents, catalysts & solvents 2

HCID 345198Adams' catalystCatalystHCID 702EthanolSolvent

Procedure

A solution of N-(3,4-dimethyl-phenyl)-4-hydroxy-3-nitrobenzamide (700 mg) in ethanol (50 mL) was hydrogenated over PtO2 at 40 psi for 3 h. The catalyst was filtered through Celite and the filtrate evaporated to give 3-amino-N-(3,4-dimethylphenyl)-4-hydroxy-benzamide as an off-white solid, mp=220-223° C.; MS (m/z) 255 (M−1).

Workup

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
filtration
The catalyst was filtered through Celite
  • customthe filtrate evaporated
  • Sources & evidence

    ORD record
    ord-ba7af0f4002547f3b2ee36e242ec2aae
    Source dataset
    uspto-grants-2012_07
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08222248B2

    Reaction notes

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