Reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]=O)=[N:6][CH:7]=1.Cl.[NH2:11][OH:12].[OH-].[Na+].Cl>C(O)C.O>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]=[N:11][OH:12])=[N:6][CH:7]=1Participants
7
Procedure
To a solution of 5-fluoro-2-formylpyridine (5.0 g, 41 mmol) and hydroxylamine hydrochloride (3.06 g, 44 mmol) in ethanol (3.2 mL) and water (9.6 mL) was added ice (18.6 g). Then a solution of NaOH (4.0 g, 100 mmol) in water (4.6 mL) was added dropwise over 10 min keeping the temperature between −5° C. and 5° C. The reaction mixture was then stirred at room temperature for 30 min. Then HCl (4 N) was added to acidify the mixture and the resulting precipitate was filtered off and washed with water to afford the title compound (4.41 g, 79%) as a light brown solid. MS: m/e=141.0 [M+H]+.
Workup
- customthe temperature between −5° C. and 5° C
- filtrationthe resulting precipitate was filtered off
- washwashed with water
Sources & evidence
- ORD record
- ord-ac51d081e44246838c3e6209b8cf1dfe
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08877783B2
Linked notes
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