Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:10](N)=[CH:9][C:4]=1C(OC)=O.Cl.N([O-])=O.[Na+].[CH2:19]([O:21][C:22]([SH:24])=S)C.[Na].[C:26](=O)([O-])[O-].[Na+].[Na+].[S-2].[Na+].[Na+].[OH-].[Na+].COS(OC)(=O)=O>O.C(OCC)(=O)C.CCCCCC>[CH3:1][O:2][C:3]1[CH:4]=[CH:9][C:10]([CH3:26])=[CH:11][C:12]=1[C:22]([O:21][CH3:19])=[S:24]Komponenten
Edukt 9
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
Alternately, combine methyl 2-methoxy-5-aminobenzoate (1.0 g, 5.6 mmol) and 12 M aqueous hydrochloric acid solution (1.2 g and cool in an ice bath. Add a solution of sodium nitrite (0.37 g, 5.3 mmol) in water (3 mL). After 1.5 hours, add ethyl xanthic acid, sodium salt (0.76 g, 6.3 mmol) and sodium carbonate (0.67 g, 6.3 mmol). After 2 hours, evaporate in vacuo and add sodium sulfide (0.69 g, 2.7 mmol) and a 1 M aqueous sodium hydroxide solution (10 mL). After 4 hours, add dimethylsulfate and heat to reflux. After 24 hours, cool to ambient temperature, acidify with 12 M hydrochloric acid solution and extract with ethyl acetate. Separate the organic layer, extract with brine, dry over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with ethyl acetate/hexane 2/1 to give methyl 2-methoxy-5-methylthiobenzoate. Elemental Analysis calculated for C9H12O3S: C, 54.53; H, 5.08. Found: C, 54.64; H, 4.95.
Aufarbeitung
- temperaturecool in an ice bath
- waitAfter 2 hours
- customevaporate in vacuo
- waitAfter 4 hours
- temperatureheat to reflux
- waitAfter 24 hours
- extractionextract with ethyl acetate
- customSeparate the organic layer
- extractionextract with brine
- dry with materialdry over Na2SO4
- filtrationfilter
- customevaporate in vacuo
- customto give a residue
Quellen und Nachweise
- ORD-Eintrag
- ord-92c476e1fc114bf59ed2b16fd3a42c1d
- Quelldatensatz
- uspto-grants-2001_04
- Patentnummer
- US06211199B1
Verknüpfte Notizen
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