Reaktion #1107
ord-61a0177588e440db829d21a8578b91c1
Reaktionsgleichung
4-(4-tert-butylanilino)-3-methoxy-2-methylpyridine
→
4-(4-tert-Butylcyclohexylamino)-3-methoxy-2-methylpyridine
Reagenzien
Keine
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Sonstigeare hydrogenated at room temperature
- 2Sonstigenormal pressure until absorption of hydrogen
- 3FiltrationAfter filtering
- 4Einengenconcentrating 1 g of syrup
Vorschrift
1 g of 4-(4-tert-butylanilino)-3-methoxy-2-methylpyridine in 20 ml of methanol, 3.7 ml of 2N HCl and 1.3 ml of water are hydrogenated at room temperature and normal pressure until absorption of hydrogen has ended using 1 g of rhodium on alumina (5% strength). After filtering and concentrating 1 g of syrup remains=100% isomer mixture.