Acetone → S 38093-2

HRID 1848332Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1848332
[CH2:1]1[C@H:5]2[CH2:6][CH2:7][CH2:8][C@H:4]2[CH2:3][N:2]1[CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:21]=[CH:20][C:16]([C:17]([NH2:19])=[O:18])=[CH:15][CH:14]=1.CC(C)=O.[ClH:26]>O>[ClH:26].[CH2:1]1[C@H:5]2[CH2:6][CH2:7][CH2:8][C@H:4]2[CH2:3][N:2]1[CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:14]=[CH:15][C:16]([C:17]([NH2:19])=[O:18])=[CH:20][CH:21]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

16.49 kg of 4-{3-[cis-hexahydrocyclopenta[c]pyrrol-2(1H)-yl]propoxy}benzamide, 16.36 kg of acetone, 6.76 kg of concentrated aqueous hydrochloric acid and 18.96 kg of water are introduced into a reactor. The mixture is stirred and heated at 50° C. for 1 hour. The mixture is then filtered in the hot state into a second reactor containing 57.67 kg of acetone and 1.65 kg of water. The mixture is then brought to reflux and 73.32 kg of acetone are added. Reflux is maintained for 10 minutes and then cooling to 0° C. is carried out. The product is filtered off and the solid obtained is washed with acetone. The product is obtained in the form of a powder in a yield of 85% and with a chemical purity greater than 99%.

Aufarbeitung

  1. filtrationThe mixture is then filtered in the hot state into a second reactor
  2. additioncontaining 57.67 kg of acetone and 1.65 kg of water
  3. temperatureto reflux
  4. addition73.32 kg of acetone are added
  5. temperatureReflux
  6. temperatureis maintained for 10 minutes
  7. temperaturecooling to 0° C.
  8. filtrationThe product is filtered off
  9. customthe solid obtained
  10. washis washed with acetone
  11. customThe product is obtained in the form of a powder in a yield of 85% and with a chemical purity greater than 99%

Quellen und Nachweise

ORD-Eintrag
ord-b6f7ad0f226949389cb41d22595152d3
Quelldatensatz
uspto-grants-2015_02
Patentnummer
US08952179B2

Notizen zur Reaktion

Wird geladen…