Triphenylphosphine → 5-Chloro-2-methoxybenzene-1-thiol
Reaktionsgleichung
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Cl:20][C:21]1[CH:22]=[CH:23][C:24]([O:31][CH3:32])=[C:25]([S:27](Cl)(=O)=O)[CH:26]=1>C1COCC1.O>[Cl:20][C:21]1[CH:22]=[CH:23][C:24]([O:31][CH3:32])=[C:25]([SH:27])[CH:26]=1Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
Triphenylphosphine (11.4 g) was added portionwise to a stirred solution of 5-chloro-2-methoxybenzenesulphonyl chloride (3.0 g) in THF (30 ml). Water (4 ml) was added and the mixture stirred at RT for 2 h, after which the reaction was diluted with water (25 ml) then 2M sodium hydroxide solution and washed with ether. The aqueous layer was acidified with 2M hydrochloric acid and extracted with ethylacetate. The organic layer was dried and evaporated under reduced pressure, yield 3.1 g.
Aufarbeitung
- wash2M sodium hydroxide solution and washed with ether
- extractionextracted with ethylacetate
- customThe organic layer was dried
- customevaporated under reduced pressure, yield 3.1 g
Quellen und Nachweise
- ORD-Eintrag
- ord-c802e92cd8f549e28bc7519933a6f9ba
- Quelldatensatz
- uspto-grants-2011_08
- Patentnummer
- US08003703B2
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