반응 #1824303

반응 방정식

sulfuric acid

sodium acetate

acetaldoxime

sodium acetate

N2

3-(trifluoromethyl)aniline

sodium nitrite

→

solid

수율 84.3%

1-[3-(trifluoromethyl)phenyl]ethanone oxime

수율 84.3%

용매

water

toluene

water

반응 조건

후처리

1. 1
   기타To a three-neck indented, Morton style flask equipped with a sidearm for thermometer
2. 2
   온도cooled to -5° C.
3. 3
   기타to give a slurry
4. 4
   workup.ADDITIONThe rate of addition
5. 5
   온도was maintained between -5 and 0° C
6. 6
   workup.STIRRINGThe mixture was stirred at that temperature for 30 min
7. 7
   workup.ADDITIONwas added
8. 8
   온도cooled to about 10° C
9. 9
   기타a two phase mixture (dark green oil and aqueous) was obtained
10. 10
    workup.STIRRINGThe mixture was stirred for 30 min before the reaction
11. 11
    기타the organic phase separated from the aqueous
12. 12
    추출The aqueous phase was extracted with another 100 mL of toluene
13. 13
    세척were washed with 15% ammonium hydroxide solution (5×20 mL)
14. 14
    세척wash
15. 15
    세척The organic phase (orange color) was washed with 20 mL of brine
16. 16
    건조dried over magnesium sulfate
17. 17
    기타Removal of volatiles on the rotovap
18. 18
    기타gave an orange oil which
19. 19
    기타upon fuirther drying on the vacuum pump

실험 절차

To a three-neck indented, Morton style flask equipped with a sidearm for thermometer charged with 80 mL (240 mmol) of 3N sulfuric acid was added 10 mL (80 mmol) of 3-(trifluoromethyl)aniline (Aldrich Chemical Co.). The resulting suspension turned into a clear solution upon heating to 65° C. The solution was stirred vigorously and cooled to -5° C. using an acetone/ice bath to give a slurry. To the slurry was added a solution of 5.85 g (84.8 mmol) of sodium nitrite in 25 mL of water. The rate of addition was carefully adjusted so the internal reaction temperature was maintained between -5 and 0° C. The mixture was stirred at that temperature for 30 min. The diazonium thus obtained appears as a thin slurry. The slurry thickened when a solution of 20 g (244 mmol) of sodium acetate in 50 mL of water was added. Meanwhile, in another flask, 19 mL (320 mmol) of acetaldoxime, 1.50 g (8 mmol) of copper (II) acetate, 0.5 g (4 mmol) of sodium sulfite, and 20 g (244 mmol) of sodium acetate were combined and cooled to about 10° C. To this solution was added via a cannula or additional funnel the diazonium mixture. Immediate gas (N2) evolution was observed, and a two phase mixture (dark green oil and aqueous) was obtained. The mixture was stirred for 30 min before the reaction was worked up. To the mixture was added about 300 mL of toluene and the organic phase separated from the aqueous. The aqueous phase was extracted with another 100 mL of toluene. The combined toluene extracts (greenish color) were washed with 15% ammonium hydroxide solution (5×20 mL). Analysis using copper test strips from EM Science indicated the copper (I/II) content to be less than 10 ppm as compared to greater than 100 ppm before the ammonium hydroxide wash. The organic phase (orange color) was washed with 20 mL of brine and dried over magnesium sulfate. Removal of volatiles on the rotovap gave an orange oil which turned into a semi-solid upon fuirther drying on the vacuum pump to give 13.7 g (84%) of a solid product. In the analytical assay, it was found to contain 58.9% of the desired oxime product.

출처