Hydrochloric Acid → HCID 59119394, compound
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
- customat 25-30° C.
- additionwas added
- stirringThe reaction was stirred for 2 h
- additionwas added
- customat 25-30° C.
- extractionextracted with Et2O
- washThe combined organic solution was washed with brine
- dry with materialdried (MgSO4)
- filtrationfiltered
- concentrationconcentrated
- 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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