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Sodium Hydroxide → 2-Methyl-4-((2-methylbenzoyl)amino)benzoic acid

HRID 2389242
Notes
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Reaction equation

HRID 2389242 reaction equation
[CH3:1][C:2]1[CH:17]=[CH:16][CH:15]=[CH:14][C:3]=1[C:4]([NH:6][C:7]1[CH:8]=[C:9]([CH3:13])[CH:10]=[CH:11][CH:12]=1)=[O:5].[Cl-].[Al+3].[Cl-].[Cl-].[C:22](Cl)(=[O:26])C(Cl)=O.[OH-:28].[Na+]>C(Cl)Cl.C1(C)C=CC=CC=1>[CH3:13][C:9]1[CH:8]=[C:7]([NH:6][C:4](=[O:5])[C:3]2[CH:14]=[CH:15][CH:16]=[CH:17][C:2]=2[CH3:1])[CH:12]=[CH:11][C:10]=1[C:22]([OH:26])=[O:28]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 14798Sodium HydroxideHCID 65578Oxalyl chlorideHCID 952902-Methyl-N-(m-tolyl)benzamideHCID 6451240Aluminum(III) Chloride

Product 1

HCID 251921172-Methyl-4-((2-methylbenzoyl)amino)benzoic acidYield 65.8%

Reagents, catalysts & solvents 2

HCID 1140
Toluene
Solvent
HCID 6344DichloromethaneSolvent2×

Conditions

Temperature
3 °C

Procedure

To a solution of 3-(2-methylbenzoylamino)toluene (50.0 g, 0.222 mole) in methylene chloride (50 mL) which is cooled to 3° C. is added aluminum chloride (88.8 g, 0.666 mole) under nitrogen atmosphere over a period of about 10 minutes. The mixture is cooled to 3° C., and thereto is added dropwise oxalyl chloride (25.2 mL, 0.289 mole) at 3-7° C. The mixture is stirred at 2-7° C. for 5 hours. After confirming the disappearance of the starting materials, the reaction mixture is diluted with methylene chloride (100 mL), and thereto is added ice water to quench the reaction. After distilling off methylene chloride, the resulting aqueous suspension is refluxed for 30 minutes and then cooled to room temperature. The resulting crystals are separated by filtration and the wet crystals are dried at 60° C. to give the crude product (58.33 g). To the crude product (29.17 g) are added 2.5 mol/L aqueous sodium hydroxide solution (400 mL) and toluene (100 mL), and insoluble materials are removed by filtration and then separated into two layers. The aqueous layer is washed twice with toluene (100 mL) and neutralized with 6 mol/L hydrochloric acid (300 mL). The precipitated crystals are separated by filtration and dried at 60° C. and then recrystallized from methanol (540 mL) to give the desired product (19.67 g, yield 65.8%, purity by HPLC 99.4%).

Workup

  1. customto quench
  2. customthe reaction
  3. distillationAfter distilling off methylene chloride
  4. temperaturethe resulting aqueous suspension is refluxed for 30 minutes
  5. temperaturecooled to room temperature
  6. customThe resulting crystals are separated by filtration
  7. customthe wet crystals are dried at 60° C.
  8. customto give the crude product (58.33 g)
  9. customare removed by filtration
  10. customseparated into two layers
  11. washThe aqueous layer is washed twice with toluene (100 mL)
  12. customThe precipitated crystals are separated by filtration
  13. customdried at 60° C.
  14. customrecrystallized from methanol (540 mL)

Sources & evidence

ORD record
ord-414c8eb31bd84c2e93cbda62e537901a
Source dataset
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08273735B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes