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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860525Generated: October 26, 2026

Methanol → Dexmethylphenidate

https://huagongshe.com/reaction/1860525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactantmethyl (S)-phenyl((R)-piperidin-2-yl)acetateHCID 6101852—
Reactant(+)-di-toluoyl-D-tartaric acidHCID 129858806—
SolventAcetoneHCID 180—
ProductDexmethylphenidateHCID 154101121.5%
Productditoluoyl-D-tartrateHCID 131722594—

Reaction Steps

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 the ditoluoyl-D-tartrate salt of l-threo-methylphenidate as a solid, dry form (4.508 g, 50.5% yield, 88% ee).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531489B2
Source datasetuspto-grants-2003_03
ORD IDord-2759d53622de4762bbfd2cadc66d7f14
Source noteuspto-grants-2003_03