Acetic Anhydride → HCID 136378652, Verbindung
Reaktionsgleichung
[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([OH:8])[C:3]=1[C:9](=[N:12][OH:13])[CH2:10][CH3:11].[C:14](OC(=O)C)(=[O:16])[CH3:15]>>[C:14]([O:13][N:12]=[C:9]([C:3]1[C:4]([OH:8])=[CH:5][CH:6]=[CH:7][C:2]=1[OH:1])[CH2:10][CH3:11])(=[O:16])[CH3:15]Komponenten
3
Versuchsvorschrift
1-(2,6-dihydroxyphenyl)-1-propanone oxime (Intermediate 29, 716 mg) was stirred in acetic anhydride (2.24 ml, 23.7 mmol) at room temperature for 1 hour. After removal of the volatiles, the residue was washed with water, filtered and dried. The crude compound was charged on a silica gel column (Biotage SP1 system) and eluted with Cyclohexane/EtOAc (from 100/0 to all 0/100) to afford the title compound (269 mg).
Aufarbeitung
- customAfter removal of the volatiles
- washthe residue was washed with water
- filtrationfiltered
- customdried
- additionThe crude compound was charged on a silica gel column (Biotage SP1 system)
- washeluted with Cyclohexane/EtOAc (from 100/0 to all 0/100)
Quellen und Nachweise
- ORD-Eintrag
- ord-62ce0eca3bda4c52840c4cf170ea354d
- Quelldatensatz
- uspto-grants-2016_05
- Patentnummer
- US09346790B2
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