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4-Azidomethyl-2-(2-methylphenyl)benzoic acid methyl ester → 4-Aminomethyl-2-(2-methylphenyl)benzoic acid methyl ester

HRID 383161
Notes
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Reaction equation

HRID 383161 reaction equation
[CH3:1][O:2][C:3](=[O:21])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][N:11]=[N+]=[N-])=[CH:6][C:5]=1[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[CH3:20]>CO.Cl>[CH3:1][O:2][C:3](=[O:21])[C:4]1[CH:9]=[CH:8][C:7]([CH2:10][NH2:11])=[CH:6][C:5]=1[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[CH3:20]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 206998904-Azidomethyl-2-(2-methylphenyl)benzoic acid methyl ester

Product 1

HCID 206998884-Aminomethyl-2-(2-methylphenyl)benzoic acid methyl esterYield 30.1%

Reagents, catalysts & solvents 2

HCID 313Hydrochloric AcidCatalystHCID 887MethanolSolvent

Procedure

To a flask at ambient temperature under N2 containing 10% palladium on carbon catalyst (1.0 g) was added a solution of 4-azidomethyl-2-(2-methylphenyl)benzoic acid methyl ester (5.00 g, 17.8 mmol), prepared as in Example 1191A, in MeOH (75 mL). Two drops of conc. HCl added, and reaction stirred vigorously overnight under an atmosphere of H2. Catalyst filtered off through celite and washed with MeOH. Filtrate concentrated in vacuo, and residue taken up in an aqueous 4N NaOH solution. Aqueous solution extracted with CHCl3 (3×), and extracts dried with Na2SO4, filtered, and concentrated in vacuo to afford the desired product (1.37 g, 30%). m/e (DCI) 256 (MH+)

Workup

  1. additionTo a flask at ambient temperature under N2 containing 10% palladium on carbon catalyst (1.0 g) was added
  2. customreaction
  3. filtrationCatalyst filtered off through celite
  4. washwashed with MeOH
  5. concentrationFiltrate concentrated in vacuo, and residue
  6. extractionAqueous solution extracted with CHCl3 (3×), and extracts
  7. dry with materialdried with Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-0f8b198dd3d34025bdbea41c1ea81023
Source dataset
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06310095B1

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes