HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Toluenesulfonylhydrazide → Methylphenidate Hydrochloride Impurity 16
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Toluenesulfonylhydrazide | HCID 15303 | — |
| Reactant | 1-Phenyl-2-(piperidin-1-yl)ethane-1,2-dione | HCID 10965965 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methylphenidate Hydrochloride Impurity 16 | HCID 85395106 | 90.6% |
Reaction Steps
A solution of 98% sulfuric acid (121.7 g, 1.22 mol, 0.02 eq) in abs ethanol (1.0 L) was added dropwise to a stirred mixture of 1-(phenylglyoxylyl)piperidine (17.58 Kg, 80.9 mol, 1 eq), p-toluenesulfonhydrazide (16.20 Kg, 87.0 mol, 1.08 eq) and abs ethanol (50 L) at 20–30° C. The obtained mixture was stirred under reflux conditions until 1-(phenylglyoxylyl)piperidine disappeared (˜7 hours, TLC control). The mixture was stirred for 1 hour at 20–30° C. and for 1 hour at 0–5° C. The precipitated solid was filtered off, washed on the filter with cold methanol and cold hexane and dried under reduced pressure to a constant weight to yield 28.25 Kg (90.6%) of 1-(phenylglyoxylyl)piperidine p-toluenesulfonylhydrazone with 99.9% purity by HPLC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07002016B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-a104960a239e4c24b520dc239cb763af |
| Source note | uspto-grants-2006_02 |