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Water → Methyl 3-amino-5-(hydroxymethyl)benzoate

HRID 49313
Notes
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Reaction equation

HRID 49313 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[C:11]([C:13]([O:15][CH3:16])=[O:14])[CH:12]=1)[C:7](O)=[O:8])([O-])=O.O.C(=O)([O-])[O-].[K+].[K+]>C1COCC1>[NH2:1][C:4]1[CH:12]=[C:11]([CH:10]=[C:6]([CH2:7][OH:8])[CH:5]=1)[C:13]([O:15][CH3:16])=[O:14]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 962WaterHCID 11430Potassium CarbonateHCID 747761,3-Benzenedicarboxylic acid, 5-nitro-, 1-methyl ester

Product 1

HCID 10535399Methyl 3-amino-5-(hydroxymethyl)benzoateYield 93.6%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

85 g of 3-nitro-5-methoxycarbonylbenzoic acid was dissolved in 200 ml of THF under a flow of nitrogen, and 43.4 ml of borane dimethylsulfide complex was added with stirring under ice-cooling. After stirring for 18 hours, 200 ml of water was added, and then 96 g of potassium carbonate was added. It was extracted with ethyl acetate, and theorganic layer was washed with salt solution. After drying with magnesium sulfate, the resulting solid was dissolved in 800 ml of ethyl acetate, 750 mg of 10% Pd/C was added, and stirring was continued under the flow of hydrogen. After the reaction was completed, it was subjected to the filtration, and then the filtrate was concentrated to produce 64 g of the title compound.

Workup

  1. additionwas added
  2. temperaturecooling
  3. stirringAfter stirring for 18 hours
  4. extractionIt was extracted with ethyl acetate, and theorganic layer
  5. washwas washed with salt solution
  6. dry with materialAfter drying with magnesium sulfate
  7. dissolutionthe resulting solid was dissolved in 800 ml of ethyl acetate
  8. addition750 mg of 10% Pd/C was added
  9. stirringstirring
  10. filtrationit was subjected to the filtration
  11. concentrationthe filtrate was concentrated

Sources & evidence

ORD record
ord-39ab0bf8396c4e4589cc7a8137c09994
Source dataset
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06706745B1

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes