Methanesulfonic Acid → decyl nicotinate N-oxide

Nicotinic acid N-oxide (5.00 g, 36 mmol), decyl alcohol (5.86 g, 37 mmol) and methanesulfonic acid (3.70 g, 38.5 mmol) were stirred and heated to reflux in toluene (50 mL), in a flask equipped with a condenser and a Dean-Stark trap for 19 hours. The rection mixture was then cooled, diluted with ether and washed successively with water, aqueous sodium bicarbonate and brine. The toluene/ether solution was then dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was recrystallized from ligroine (100 mL) to give 7.50 g (27 mmol) of decyl nicotinate N-oxide, mp 80.5° C.

1. temperatureheated
2. customequipped with a condenser
3. temperatureThe rection mixture was then cooled
4. washwashed successively with water, aqueous sodium bicarbonate and brine
5. dry with materialThe toluene/ether solution was then dried over anhydrous magnesium sulfate
6. filtrationfiltered
7. customevaporated under reduced pressure
8. customThe residue was recrystallized from ligroine (100 mL)

ORD-Eintrag

ord-f8d86c69f08f4cb1a8a3946aece0ed25

Quelldatensatz

uspto-grants-1992_08

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US05141839