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Sodium Hydroxide → Methyl 2-amino-6-iodobenzoate

HRID 3124
Notes
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Reaction equation

HRID 3124 reaction equation
[OH-].[Na+].[I:3][C:4]1[C:9]2[C:10](=[O:15])[O:11][C:12](=O)[NH:13][C:8]=2[CH:7]=[CH:6][CH:5]=1>CO.[OH-].[Na+]>[NH2:13][C:8]1[CH:7]=[CH:6][CH:5]=[C:4]([I:3])[C:9]=1[C:10]([O:11][CH3:12])=[O:15]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 14798Sodium HydroxideHCID 106848156-(Iodo)isatoic anhydride

Product 1

HCID 11011279Methyl 2-amino-6-iodobenzoateYield 78.4%

Reagents, catalysts & solvents 2

HCID 14798Sodium HydroxideCatalystHCID 887MethanolSolvent

Conditions

Temperature
60 °C

Procedure

To a stirred solution of sodium hydroxide (0.35 g, 8.8 mM) in methanol (31 mL) was added 5-iodo-2H-3,1-benzoxazine-2,4(1H)-dione (18.5 g, 64.0 mM). The mixture was heated at 60° C. for 1.5 hr. An additional quantitiy of sodium hydroxide (0.10 g, 2.5 mM) was added to the reaction mixture and stirring at 60° C. was continued for an additonal 1 hr. After cooling to room temperature, the reaction mixture was concentrated and the residue was taken up in ethyl acetate. The ethyl acetate was washed successively with water, brine, dilute aqueous sodium hydroxide, and water. After drying over MgSO4, the ethyl acetate was filtered and concentrated to leave (13.9 g, 78.4%) of the title ester as a brown oil; MS(CI): 278 (M+H).

Workup

  1. temperatureAfter cooling to room temperature
  2. concentrationthe reaction mixture was concentrated
  3. washThe ethyl acetate was washed successively with water, brine, dilute aqueous sodium hydroxide, and water
  4. dry with materialAfter drying over MgSO4
  5. filtrationthe ethyl acetate was filtered
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-b6d9760dfaec4627a210e1ab02e7806c
Source dataset
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05733910

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes