Nitric Acid → 3-Methyl-5-isoxazolecarboxylic acid
Reaction equation
[CH2:1]([CH2:5][C:6](=O)[CH3:7])[C:2](C)=[O:3].[N+:9]([O-:12])(O)=O.[OH2:13]>>[CH3:7][C:6]1[O:12][N:9]=[C:1]([C:2]([OH:13])=[O:3])[CH:5]=1Participants
4
Procedure
A mixture of acetonylacetone (10 g, 88 mmol) and nitric acid (sp. gr. 1.42)/water (2:3) (50 ml) was cautiously brought to reflux under a stream of nitrogen and boiled for 1 h. The solution was cooled to room temperature and aged overnight. The resultant solid was collected by filtration, washed with chilled water (2×7 ml) and hexane, and dried in vacuo to give the title-acid (4.4 g, 40%), 1H NMR (CDCl3) δ 2.50 (3H, d, J=0.8 Hz, Me), 6.41 (1H, d, J=0.8 Hz, Ar—H).
Workup
- temperatureto reflux under a stream of nitrogen
- filtrationThe resultant solid was collected by filtration
- washwashed with chilled water (2×7 ml) and hexane
- customdried in vacuo
- customto give the title-acid (4.4 g, 40%), 1H NMR (CDCl3) δ 2.50 (3H, d, J=0.8 Hz, Me), 6.41 (1H, d, J=0.8 Hz, Ar—H)
Sources & evidence
- ORD record
- ord-c1c56a0ae6b344cb83aae5085a3596d7
- Source dataset
- uspto-grants-2003_03
- Patent number
- US06534505B2
Reaction notes
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