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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1374130생성일: 2026년 10월 26일

Methanol → Dexmethylphenidate

https://huagongshe.com/reaction/1374130

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물methyl (S)-phenyl((R)-piperidin-2-yl)acetateHCID 6101852—
반응물(+)-di-toluoyl-D-tartaric acidHCID 129858806—
용매AcetoneHCID 180—
생성물DexmethylphenidateHCID 15410197%
생성물ditoluoyl-D-tartrateHCID 131722594—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07164025B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-eb4b30fa4fec40fdb01f055860b52701
출처 메모uspto-grants-2007_01