Reaktionsgleichung
Cl.[N:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8][C:9]([OH:11])=O)[CH:3]=1.[P:12]([OH:15])([OH:14])[OH:13].[P:16](=O)([OH:19])([OH:18])[OH:17].P(Cl)(Cl)(Cl)=O>O.C1(C)C=CC=CC=1>[CH:6]1[CH:7]=[N:2][CH:3]=[C:4]([CH2:8][C:9]([P:16]([OH:19])([OH:18])=[O:17])([P:12]([OH:15])([OH:14])=[O:13])[OH:11])[CH:5]=1Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 90 °C
Versuchsvorschrift
A 500 ml cylindrical reactor equipped with a mechanical stirrer, a thermometer, a reflux condenser and a dropping funnel, was charged with 3-pyridine acetic acid hydrochloride (6.94 g, 0.04 mole), phosphorous acid (9.84 g, 0.12 mole), ortho-phosphoric acid (11.80 g, 0.12 mole) and toluene (50 ml). The suspension was heated to 90° C. and phosphorous oxychloride (11.2 ml, 0.12 mole) was added dropwise during 20 minutes. The reaction mixture was then heated to 95° C. for 20.5 hours. Water (50 ml) was added after cooling the reaction mixture to 80° C. The mixture was stirred vigorously until the solidified product dissolved completely. The toluene and the aqueous phases were separated and the aqueous phase was heated at 95° C. for 5.5 hours. The aqueous phase was cooled to 25° C. and absolute ethanol (50 ml) was added to precipitate the final product. The suspension was cooled to 5° C. for 1 hour. The white product was filtered, washed with absolute ethanol (2×20 ml) and dried at 65° C. for 5 hours to obtain 7.70 g (68%) of risedronic acid monohydrate.
Aufarbeitung
- customA 500 ml cylindrical reactor equipped with a mechanical stirrer
- temperatureThe reaction mixture was then heated to 95° C. for 20.5 hours
- temperatureafter cooling the reaction mixture to 80° C
- dissolutiondissolved completely
- customThe toluene and the aqueous phases were separated
- temperaturethe aqueous phase was heated at 95° C. for 5.5 hours
- temperatureThe aqueous phase was cooled to 25° C.
- additionabsolute ethanol (50 ml) was added
- customto precipitate the final product
- temperatureThe suspension was cooled to 5° C. for 1 hour
- filtrationThe white product was filtered
- washwashed with absolute ethanol (2×20 ml)
- customdried at 65° C. for 5 hours
Quellen und Nachweise
- ORD-Eintrag
- ord-90cb7c4ff7244ae089de09e3826e2728
- Quelldatensatz
- uspto-grants-2006_05
- Patentnummer
- US07038083B2
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