Reaktion #1199565

Reaktionsgleichung

water

2-(N-butylamino)-4-methyloxazole

triethylamine

isobutyryl chloride

→

2-(N-butyl isobutyramido)-4-methyloxazole

Ausbeute 80.0%

Lösungsmittel

benzene

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGAfter stirring for a further hour the organic phase
2. 2
   Sonstigewas separated
3. 3
   Extraktionthe aqueous phase extracted twice in ether
4. 4
   ExtraktionThe combined extract
5. 5
   Waschenwas washed successively with 2N hydrochloric acid (2 × 500 c.c.), 10% sodium carbonate solution (2 × 500 c.c.), and saturated brine (2 × 500 c.c.)
6. 6
   SonstigeEvaporation of the dried organic phase
7. 7
   Sonstigegave an oil, which
8. 8
   workup.DISTILLATIONwas distilled

Vorschrift

2-(N-butylamino)-4-methyloxazole (106.7 g., 0.69 m.) and triethylamine (110 g., 0.77 m.) were stirred together in dry benzene (1500 c.c.) during the addition of isobutyryl chloride (81.0 g., 0.76 m.). The mixture was stirred at room temperature for 15 hours and then water (1 liter) was added. After stirring for a further hour the organic phase was separated, and the aqueous phase extracted twice in ether. The combined extract was washed successively with 2N hydrochloric acid (2 × 500 c.c.), 10% sodium carbonate solution (2 × 500 c.c.), and saturated brine (2 × 500 c.c.). Evaporation of the dried organic phase gave an oil, which was distilled to give 2-(N-butyl isobutyramido)-4-methyloxazole, (118 g., 80%), b.p. 75°-76° C/0.15 mm., which existed as an oil at room temperature but crystallised on cooling to 0° C.

Quelle