Reaktion #49973

ord-dd733e1a9b8e43559d9f6fc67ca8840f

Reaktionsgleichung

[O-][n+]1c(Cl)cccc1Cl
2,6-dichloropyridine N-oxide
Sc1ccccc1
thiophenol
[Na+].[OH-]
sodium hydroxide
[O-][n+]1c(Cl)cccc1-c1cccs1
2-chloro-6-thiophenylpyridine N-oxide

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The 1.64 g (0.010 moles) of 2,6-dichloropyridine N-oxide and 1.11 g (99%) (0.010 moles) of thiophenol was reacted with 0.400 g (0.010 moles) of ground sodium hydroxide of 16.4 ml of DMSO at 80° C. for 5 hours to give 2-chloro-6-thiophenylpyridine N-oxide. It was reacted with 1.20 g (0.030 moles) of ground sodium hydroxide at 80° C. for 2.5 hours to give 1-hydroxy-6-thiophenylpyridine-2-(1H)-one. After cooling, it was added 148 ml of water and was adjusted with 6N HCl to pH 3. The precipitate was filtered, washed with water and washed with hexanes to give 1.64 g (75%). It was recrystallized from ethanol: mp 180°-181° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05424435uspto-grants-1995_06