Reaktionsgleichung
[CH2:1]([O:3][C:4]([CH:6]1[O:10][C:9]2[CH:11]=[CH:12][C:13]([CH3:15])=[CH:14][C:8]=2[O:7]1)=[O:5])[CH3:2].[C:16]1([S:22](Cl)=[O:23])[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.[Cl-].[Al+3].[Cl-].[Cl-]>ClCCCl.ClC(Cl)C>[CH2:1]([O:3][C:4]([CH:6]1[O:7][C:8]2[CH:14]=[C:13]([CH3:15])[C:12]([S:22]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)=[O:23])=[CH:11][C:9]=2[O:10]1)=[O:5])[CH3:2]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
20.8 g (0.1 mol) of 5-methyl-1,3-benzodioxole-2-carboxylic acid ethyl ester Example 2b) and 19.2 g (0.125 mol) of phenylsulphinic acid chloride are dissolved in 200 ml of 1,2-dichloroethane and cooled to 5° using an ice-bath. 13.3 g (0.1 mol) of aluminium chloride are introduced in the course of approximately 15 minutes at from 5°-10° while stirring. The mixture is stirred for a further hour in the ice-bath and is then poured out onto ice-water. The resulting emulsion is diluted with 200 ml of dichloroethane and filtered across a layer of a filter aid (for example Hyflo). The filtrate is introduced into a separating funnel and the layers are separated. The organic phase is dried over sodium sulphate, filtered and concentrated to dryness by evaporation. A light brown honey-like product, 5-phenylsulphinyl-6-methyl-1,3-benzodioxole-2-carboxylic acid ethyl ester, is obtained.
Aufarbeitung
- temperaturecooled to 5°
- additionis then poured out onto ice-water
- additionThe filtrate is introduced into a separating funnel
- customthe layers are separated
- dry with materialThe organic phase is dried over sodium sulphate
- filtrationfiltered
- concentrationconcentrated to dryness by evaporation
Quellen und Nachweise
- ORD-Eintrag
- ord-3626516582ce4e578fbdc7089df2579f
- Quelldatensatz
- uspto-grants-1986_07
- Patentnummer
- US04600709
Verknüpfte Notizen
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