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Acetic Acid → N-[4-amino-2-fluoro-5-(2-hydroxyphenoxy)phenyl]acetamide

HRID 433725
Notes
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Reaction equation

HRID 433725 reaction equation
C(O)(=O)C.[F:5][C:6]1[CH:11]=[C:10]([N+:12]([O-])=O)[C:9]([O:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[OH:22])=[CH:8][C:7]=1[NH:23][C:24](=[O:26])[CH3:25].C(OCC)(=O)C>[Fe].O>[NH2:12][C:10]1[C:9]([O:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[OH:22])=[CH:8][C:7]([NH:23][C:24](=[O:26])[CH3:25])=[C:6]([F:5])[CH:11]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 176Acetic AcidHCID 8857Ethyl AcetateHCID 21933568N-[2-fluoro-5-(2-hydroxyphenoxy)-4-nitrophenyl]acetamide

Product 1

HCID 18759282N-[4-amino-2-fluoro-5-(2-hydroxyphenoxy)phenyl]acetamideYield 82.3%

Reagents, catalysts & solvents 2

HCID 23925IronCatalyst
HCID 962
Water
Solvent
2×

Conditions

Temperature
80 °C

Procedure

Into a mixture of 25 ml of acetic acid and 25 ml of water was added 9.5 g of an iron powder, and the mixture was heated to 80° C. Into the mixture was added dropwise a solution composed of 10.0 g of N-[2-fluoro-5-(2-hydroxyphenoxy)-4-nitrophenyl]acetamide and 100 ml of ethyl acetate. The mixture was heated for 1 hour under reflux, then, poured into water, extracted with ethyl acetate, the organic layer was washed with water, and washed with saturated aqueous sodium bicarbonate, dried over magnesium sulfate, and concentrated to obtain 7.42 g of N-[4-amino-2-fluoro-5-(2-hydroxyphenoxy)phenyl]acetamide.

Workup

  1. additionInto the mixture was added dropwise a solution
  2. temperatureThe mixture was heated for 1 hour
  3. temperatureunder reflux
  4. extractionextracted with ethyl acetate
  5. washthe organic layer was washed with water
  6. washwashed with saturated aqueous sodium bicarbonate
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-8aabb13bc11c401d90a562467b478d1f
Source dataset
uspto-grants-2003_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06667413B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes