Reaktionsgleichung
[CH3:1][C@H:2]([C:13]([OH:15])=[O:14])[C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH:10]([CH3:12])[CH3:11])=[CH:5][CH:4]=1>CCCCCCC>[OH:15][C:13]([CH:2]([C:3]1[CH:4]=[CH:5][C:6]([CH2:9][CH:10]([CH3:11])[CH3:12])=[CH:7][CH:8]=1)[CH3:1])=[O:14]Komponenten
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 220 °C
Versuchsvorschrift
Racemization and Distillation of R(-)-Enriched Ibuprofen. Heptane is removed as stream 18, FIG. 1, by distillation in an evaporator at atmospheric pressure from a mixture [stream 15, FIG. 1] containing S(+)-ibuprofen (0.1912 moles, 39.43 g), R(-)-ibuprofen (0.5136 moles, 105.95 g), and heptane (ca. 390 g). During the distillation, water [30 g, stream 17] is injected into the base of the evaporator to help strip out the last traces of heptane and to minimize formation of ibuprofen ethyl ester. The molten evaporation residue [stream 33], which consists essentially of ibuprofen with an S/R ratio of 27/73, is first racemized by being heated under nitrogen at 220° C. for four (4) hours and is then distilled at about 220° C., 10 mm HgA in an evaporator to provide a distillate [stream 19] of substantially pure racemized ibuprofen (0.6907 moles, 142.48 g, S/R ratio of 47:53) and an undistilled residue [stream 20, 2.91 g] for incineration as a waste stream. Racemized ibuprofen distillate [stream 19] is recycled to the first crop crystallization of crude S(+)-ibuprofen lysinate.
Aufarbeitung
- distillationRacemization and Distillation of R(-)-Enriched Ibuprofen
- customHeptane is removed as stream 18, FIG. 1, by distillation in an evaporator at atmospheric pressure from a mixture [stream 15, FIG. 1]
- distillationDuring the distillation, water [30 g, stream 17]
- customis injected into the base of the evaporator
- customThe molten evaporation residue [stream 33], which
- distillationis then distilled at about 220° C.
- custom10 mm HgA in an evaporator
Quellen und Nachweise
- ORD-Eintrag
- ord-198c5f9078fc443ea51a00d66785f190
- Quelldatensatz
- uspto-grants-1995_03
- Patentnummer
- US05399707
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