Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374130Generated: October 25, 2026

Methanol → Dexmethylphenidate

https://huagongshe.com/reaction/1374130

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 15410197%
Productditoluoyl-D-tartrateHCID 131722594—

Reaction Steps

Resolve dl-threo-methylphenidate by the procedure described in the Example of PCT/GB97/00185 (International Publication No. WO 97/27176): 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 vacuc 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 numberUS07164025B2
Source datasetuspto-grants-2007_01
ORD IDord-eb4b30fa4fec40fdb01f055860b52701
Source noteuspto-grants-2007_01