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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1066186Erstellt: 26. Oktober 2026

Methanol → Dexmethylphenidate

https://huagongshe.com/reaction/1066186

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Eduktmethyl (S)-phenyl((R)-piperidin-2-yl)acetateHCID 6101852—
Edukt(+)-di-toluoyl-D-tartaric acidHCID 129858806—
LösungsmittelAcetoneHCID 180—
ProduktDexmethylphenidateHCID 154101121,5%
Produktditoluoyl-D-tartrateHCID 131722594—

Reaktionsschritte

Ditoluoyl-D-tartaric acid (5.033 g, 12.4 mmol) was suspended in a solution of 2% methanol in acetone (10 ml), and a solution of threo-methylphenidate (2.9 g, 12.4 mmol) in the same solvent (10 ml) was added. The solution was gently warmed to reflux whereupon all the reagents dissolved. The solution was immediately cooled and crystals began to form. The solution was allowed to stand at 4° C. for 17 hours and was then filtered. The crystals were washed with acetone (3×15 ml) and dried in vacuo to yield the ditoluoyl-D-tartrate salt of d-threo methylphenidate (3.516 g, 44.3% by weight; corresponding to 97% ee d-threo methylphenidate, as determined by chiral HPLC after salt cracking). The mother liquors were dried in vacuo to yield ditoluoyl-D-tartrate salt of l-threo-methylphenidate as a solid, dry form (4.508 g, 50.5% yield, 88% ee).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06242464B1
Quelldatensatzuspto-grants-2001_06
ORD IDord-8800611516154fea91a60faaca82eca5
Quellennotizuspto-grants-2001_06