Reaktionsgleichung
[S:1]([C:9]1[CH:14]=[CH:13][C:12](O)=[CH:11][CH:10]=1)C1C=CC(O)=CC=1.CN([CH:19]=[O:20])C>>[O:20]([C:19]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[SH:1])[C:14]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[SH:1]Komponenten
Versuchsvorschrift
4.91 g (0.0225 mol) of 4,4′-thiodiphenol was dissolved in DMF, and then an aqueous solution of 1.26 g (0.0225 mol) of NaSH was added thereto. The mixture was stirred for 24 hours. The mixture was washed with water several times and filtered, and thus oxydibenzenethiol was obtained. The oxydibenzenethiol thus obtained was dissolved in methylene chloride, and then 1.50 g (0.0148 mol) of triethylamine (TEA) was added thereto. The mixture was stirred for 10 minutes. Subsequently, 1.34 g (0.0148 mol) of acyloyl chloride was added thereto, and the mixture was stirred. After 24 hours, the mixture was washed several times with distilled water and several times with a 1 wt % aqueous hydrochloric acid solution, the organic layer was separated, and the solvent was eliminated. A residue remaining thereafter was purified by a chromatographic method and using hexane and ethyl acetate. An aqueous solution containing 0.89 g (0.0158 mol) of KOH was added thereto, 1.462 g (0.0158 mol) of epichlorohydrin was added thereto, and the mixture was stirred at normal temperature. After 36 hours, chloroform was added to the mixture to extract the product, and then the extract was washed several times with distilled water. Epichlorohydrin and the solvent were evaporated, and then a compound represented by the Formula (1-8) was separated by a chromatographic method and using hexane and ethyl acetate at a weight ratio of 2:1. The compound was purified to a purity of 99% or higher (yield: 75%).
Aufarbeitung
- washThe mixture was washed with water several times
- filtrationfiltered
Quellen und Nachweise
- ORD-Eintrag
- ord-301b3456dead4d889da5f7f06a1b8940
- Quelldatensatz
- uspto-grants-2015_08
- Patentnummer
- US09096779B2
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