Hydroxylamine → 2-Hydroxyimino-2-(3-hydroxyphenyl)acetic acid

HRID 1659683Notes

Reaction equation

HRID 1659683 reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([C:8](=O)[C:9]([OH:11])=[O:10])[CH:5]=[CH:6][CH:7]=1.[NH2:13][OH:14]>>[OH:14][N:13]=[C:8]([C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([OH:1])[CH:3]=1)[C:9]([OH:11])=[O:10]

Participants

3

Reactant 2

HCID 787HydroxylamineHCID 135480972-(3-Hydroxyphenyl)-2-oxo-ethanoic acid

Product 1

HCID 867363792-Hydroxyimino-2-(3-hydroxyphenyl)acetic acid

Procedure

2-(3-Hydroxyphenyl)glyoxylic acid (3.32 g.) and 1 N-methanol solution of hydroxylamine (45 ml.) were refluxed with stirring for 25 minutes. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in 1 N-aqueous solution of sodium hydroxide (70 ml.). An aqueous solution was washed with ether, acidified with dil. hydrochloric acid and then extracted with ethyl acetate. The extract was washed, dried and treated with an activated charcoal. The solvent was distilled off to give 2-hydroxyimino-2-(3-hydroxyphenyl)acetic acid (a mixture of syn and anti isomers) (2.9 g.).

Workup

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. dissolutionThe residue was dissolved in 1 N-aqueous solution of sodium hydroxide (70 ml.)
  3. washAn aqueous solution was washed with ether
  4. extractionextracted with ethyl acetate
  5. washThe extract was washed
  6. customdried
  7. additiontreated with an activated charcoal
  8. distillationThe solvent was distilled off

Sources & evidence

ORD record
ord-f00ed1e6b92947f38a30038e8180c400
Source dataset
uspto-grants-1981_12
Patent number
US04304770

Reaction notes

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