戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1374130作成日:2026年10月27日

Methanol → Dexmethylphenidate

https://huagongshe.com/reaction/1374130

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物methyl (S)-phenyl((R)-piperidin-2-yl)acetateHCID 6101852—
反応物(+)-di-toluoyl-D-tartaric acidHCID 129858806—
溶媒AcetoneHCID 180—
生成物DexmethylphenidateHCID 15410197%
生成物ditoluoyl-D-tartrateHCID 131722594—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07164025B2
出典データセットuspto-grants-2007_01
ORD IDord-eb4b30fa4fec40fdb01f055860b52701
出典メモuspto-grants-2007_01