Hydrochloric Acid → HCID 59119394, compound

HRID 434057Notes

Reaction equation

HRID 434057 reaction equation
[F:1][C:2]1[CH:9]=[CH:8][C:7]([I:10])=[CH:6][C:3]=1[CH:4]=O.Cl.[NH2:12][OH:13].[OH-].[Na+].Cl>O.CCO>[F:1][C:2]1[CH:9]=[CH:8][C:7]([I:10])=[CH:6][C:3]=1[CH:4]=[N:12][OH:13]

Participants

7

Procedure

To a mixture of 2-fluoro-5-iodobenzaldehyde (9.4 mmol) in H2O (5 ml), EtOH (5 ml), and ice (4.5 g) was added hydroxylamine hydrochloride (0.67 g, 10.3 mmol, 1.1 eq.). Then, 23.6 mmol of 50% NaOH (1 g in 1 ml H2O, 2.5 eq.) was added with stirring. Enough ice to keep the temperature at 25-30° C. was added. The reaction was stirred for 2 h, acidified with conc. HCl to pH 4 (ice was added to keep the temperature at 25-30° C.), and extracted with Et2O. The combined organic solution was washed with brine, dried (MgSO4), filtered, and concentrated. The residue was chromatographed on silica gel using (1-10%) ethyl acetate in hexanes to give 2-fluoro-5-iodobenzaldehyde oxime (2.06 g, 78% over 2 steps).

Workup

  1. customat 25-30° C.
  2. additionwas added
  3. stirringThe reaction was stirred for 2 h
  4. additionwas added
  5. customat 25-30° C.
  6. extractionextracted with Et2O
  7. washThe combined organic solution was washed with brine
  8. dry with materialdried (MgSO4)
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customThe residue was chromatographed on silica gel using (1-10%) ethyl acetate in hexanes

Sources & evidence

ORD record
ord-2025edfe852b46e6b13efd775ab51dd3
Source dataset
uspto-grants-2003_12
Patent number
US06670373B1

Reaction notes

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