Formic Acid → HCID 15052523, compound
Reaction equation
[NH2:1][C:2]1[CH:6]=[C:5]([CH3:7])[O:4][N:3]=1.[CH:8](O)=[O:9]>>[CH:8]([NH:1][C:2]1[CH:6]=[C:5]([CH3:7])[O:4][N:3]=1)=[O:9]Participants
3
Procedure
To 3-amino-5-methylisoxazole (10.0 g), 99% formic acid (47.0 g) is added, and the resultant mixture is refluxed for 1 hour with stirring. The reaction mixture is evaporated under reduced pressure to remove the formic acid. The residue is mixed with icy water (50 ml), and the precipitated crystals are filtered. The crystals are washed with water and dried under reduced pressure to give 3-formylamino-5-methylisoxazole (12.06 g). This substance is recrystallized from methanol to give crystals melting at 130.5° to 131° C.
Workup
- customThe reaction mixture is evaporated under reduced pressure
- customto remove the formic acid
- additionThe residue is mixed with icy water (50 ml)
- filtrationthe precipitated crystals are filtered
- washThe crystals are washed with water
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-f50e11534f6944d893bc3a593b1c9e6e
- Source dataset
- uspto-grants-1978_09
- Patent number
- US04111680
Reaction notes
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