2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 3-Tert-butyl-4-cyano-isoxazole-5-carboxylic acid ethyl ester
Reaktionsgleichung
[CH2:1]([O:3][C:4]([CH:6]1[O:10][N:9]=[C:8]([C:11]([CH3:14])([CH3:13])[CH3:12])[CH:7]1[C:15]#[N:16])=[O:5])[CH3:2].C(C1C(=O)C(Cl)=C(Cl)C(=O)C=1C#N)#N>C1(C)C=CC=CC=1>[CH2:1]([O:3][C:4]([C:6]1[O:10][N:9]=[C:8]([C:11]([CH3:13])([CH3:12])[CH3:14])[C:7]=1[C:15]#[N:16])=[O:5])[CH3:2]Komponenten
Reaktionsbedingungen
- Temperatur
- 110 °C
Versuchsvorschrift
3-tert-Butyl-4-cyano-4,5-dihydro-isoxazole-5-carboxylic acid ethyl ester (1.51 g, 2.56 mmol corrected for the measured purity, prepared as described in the previous step) was dissolved in toluene (10 mL) and DDQ (2.41 g, 10.6 mmol) was added as a solid. The resulting mixture was heated to 110° C. for 16 h and then cooled to room temperature and diluted with hexanes (2 mL). The resulting suspension was filtered and the precipitate was washed once with toluene (4 mL). The filtrates were combined and concentrated under reduced pressure. The resulting residue was chromatographed on a 24-g SiO2 pre-packed column eluting with 0:1-1:4 EtOAc-hexanes to yield 3-tert-butyl-4-cyano-isoxazole-5-carboxylic acid ethyl ester. 1H-NMR (400 MHz, CDCl3) δ: 4.52 (q, J=7.1 Hz, 2H), 1.49 (s, 9H), 1.43-1.48 (t, J=7.1 Hz, 3H).
Aufarbeitung
- customprepared
- temperaturecooled to room temperature
- filtrationThe resulting suspension was filtered
- washthe precipitate was washed once with toluene (4 mL)
- concentrationconcentrated under reduced pressure
- customThe resulting residue was chromatographed on a 24-g SiO2 pre-packed column
- washeluting with 0:1-1:4 EtOAc-hexanes
Quellen und Nachweise
- ORD-Eintrag
- ord-4771b36d99a740d1847d928a81d205d0
- Quelldatensatz
- uspto-grants-2015_05
- Patentnummer
- US09023846B2
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