2-Naphthalenethiol → 3-(Naphth-2-ylthio)propiophenone
Reaktionsgleichung
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[SH:11].Br[CH2:13][CH2:14][C:15]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[O:16].[OH-].[Na+]>CN(C)C=O>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[S:11][CH2:13][CH2:14][C:15]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[O:16]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 2-naphthalenethiol (12.94 g), 3-bromopropiophenone (17.35 g), cuprous oxide (5.83 g), sodium hydroxide (3.24 g) and dimethylformamide (130 ml) was heated to reflux for 18 hours. The mixture was concentrated and the residue was partitioned between diethyl ether and water. The organic phase was dried (MgSO4) and evaporated. The residue was dissolved in a mixture of ethyl acetate and hexane and treated with charcoal. The solution was filtered and evaporated. The residue was recrystallised from a mixture of methanol and water to give 3-(naphth-2-ylthio)propiophenone (5.23 g, 22%), m.p. 90°-91° C.
Aufarbeitung
- temperaturewas heated
- temperatureto reflux for 18 hours
- concentrationThe mixture was concentrated
- customthe residue was partitioned between diethyl ether and water
- dry with materialThe organic phase was dried (MgSO4)
- customevaporated
- dissolutionThe residue was dissolved in a mixture of ethyl acetate and hexane
- additiontreated with charcoal
- filtrationThe solution was filtered
- customevaporated
- customThe residue was recrystallised from a mixture of methanol and water
Quellen und Nachweise
- ORD-Eintrag
- ord-3feff9f4105649b3a60f2d7dec1ba684
- Quelldatensatz
- uspto-grants-1992_02
- Patentnummer
- US05089513
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