Hydrochloric Acid → HCID 54161649, compound
Reaction equation
[NH2:1][C:2]1[O:6][N:5]=[C:4]([C:7](=[N:13][O:14][CH3:15])[C:8]([O:10]CC)=[O:9])[N:3]=1.[OH-].[Na+].Cl.[Cl-].[Na+]>>[NH2:1][C:2]1[O:6][N:5]=[C:4]([C:7](=[N:13][O:14][CH3:15])[C:8]([OH:10])=[O:9])[N:3]=1Participants
5
Procedure
Ethyl 2-(5-amino-1,2,4-oxadiazol-3-yl)-2-methoxyiminoacetate (syn isomer) (2.5 g) was added to 1N aqueous sodium hydroxide (14 ml), and the solution was stirred at ambient temperature for an hour. The reaction mixture was adjusted to pH 1.8 with 10% hydrochloric acid, salted out with sodium chloride, and then extracted with a mixture of ethyl acetate and tetrahydrofuran. After drying over anhydrous magnesium sulfate, the extract was evaporated to dryness to give a residue, which was washed with diisopropyl ether to obtain 2-(5-amino-1,2,4-oxadiazol-3-yl)-2-methoxyiminoacetic acid (syn isomer) (2.0 g).
Workup
- extractionextracted with a mixture of ethyl acetate and tetrahydrofuran
- dry with materialAfter drying over anhydrous magnesium sulfate
- customthe extract was evaporated to dryness
- customto give a residue, which
- washwas washed with diisopropyl ether
Sources & evidence
- ORD record
- ord-3aef02dc31854bb1a27a72110bb6a06e
- Source dataset
- uspto-grants-1992_05
- Patent number
- US05110921
Reaction notes
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