Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[O:8][C:7]([CH3:13])([CH3:12])[C:6]([CH2:16][OH:17])([CH2:14]O)[C:5]2=[O:18].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N(C(OC(C)C)=O)=NC(OC(C)C)=O>C1COCC1.C1(C)C=CC=CC=1.CN(C)C(=S)[S-].CN(C)C(=S)[S-].[Zn+2]>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[O:8][C:7]([CH3:13])([CH3:12])[C:6]1([CH2:16][O:17][CH2:14]1)[C:5]2=[O:18]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Versuchsvorschrift
To a mixture of 6-bromo-3,3-bis(hydroxymethyl)-2,2-dimethyl-2,3-dihydro-4H-chromen-4-one (6.76 g, 21.4 mmol), zinc bis(dimethyldithiocarbamate) (26.2 g, 85.8 mmol) and triphenylphosphine (8.44 g, 32.2 mmol) in THF (0.20 L) was added diisopropyl azodicarboxylate (1.9 M solution in toluene, 16.9 mL, 32.2 mmol) in an ice-water bath. The mixture was stirred overnight at ambient temperature. The mixture was diluted with toluene (0.20 L), and the mixture was filtered off. The filtrate was washed with 1 M aqueous NaOH (three times), water and brine, dried over MgSO4 and filtered. The filtrate was evaporated to give a crude product. The crude product was purified with column chromatography on silica gel (Hexane-EtOAc, a linear gradient of EtOAc from 0 to 20%) to afford 6-bromo-2,2-dimethyl-4H-spiro[chromene-3,3′-oxetan]-4-one (2.22 g).
Aufarbeitung
- filtrationthe mixture was filtered off
- washThe filtrate was washed with 1 M aqueous NaOH (three times), water and brine
- dry with materialdried over MgSO4
- filtrationfiltered
- customThe filtrate was evaporated
- customto give a crude product
- customThe crude product was purified with column chromatography on silica gel (Hexane-EtOAc
Quellen und Nachweise
- ORD-Eintrag
- ord-6c66971247fc4a2391c9870c1af9bea4
- Quelldatensatz
- uspto-grants-2016_01
- Patentnummer
- US09242973B2
Verknüpfte Notizen
Wird geladen…