2-Phenylbutyric Acid → 4'-(1-Oxo-2-phenylbutyl)methanesulfonanilide

HRID 1414266

Reaktionsgleichung

Reaktionsgleichung von HRID 1414266
[CH3:1][S:2]([NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)(=[O:4])=[O:3].[C:12]1([CH:18]([CH2:22][CH3:23])[C:19](O)=[O:20])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>O>[O:20]=[C:19]([C:9]1[CH:8]=[CH:7][C:6]([NH:5][S:2]([CH3:1])(=[O:4])=[O:3])=[CH:11][CH:10]=1)[CH:18]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH2:22][CH3:23]

Komponenten

4

Versuchsvorschrift

Methanesulfonanilide (40 g., 0.234 mole) is added over a 10 minute period with stirring to polyphosphoric acid (400 g.) heated to 90°-100°C. Heating and stirring are continued for additional 10 minutes, at which time 2-phenylbutanoic acid (36.0 g., 0.219 mole) is added portionwise during 20 minutes. After heating and stirring for 10 minutes, the solution is poured into water (600 ml.) and ice (400 g.) with stirring. The water is decanted and ethyl ether (200 ml.) is added to the remaining oil with stirring. After cooling in ice water, the product crystallizes and is collected: 18.4 g., m.p. 143°-147°C. Recrystallization from isopropanol yields 15.7 g. (23% yield), m.p. 148°-150°C.

Aufarbeitung

  1. temperatureheated to 90°-100°C
  2. temperatureHeating
  3. additionis added portionwise during 20 minutes
  4. temperatureAfter heating
  5. stirringstirring for 10 minutes
  6. stirringwith stirring
  7. customThe water is decanted
  8. additionethyl ether (200 ml.) is added to the remaining oil
  9. stirringwith stirring
  10. temperatureAfter cooling in ice water
  11. customthe product crystallizes
  12. customis collected
  13. customRecrystallization from isopropanol
  14. customyields 15.7 g

Quellen und Nachweise

ORD-Eintrag
ord-58cc82de06ba4bb5a678ac389eed67c7
Quelldatensatz
uspto-grants-1977_01
Patentnummer
US04001229

Verknüpfte Notizen

Wird geladen…