HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Methylnicotinic acid Hydrochloride → 4-Methylpiperidine-3-carboxylic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Methylnicotinic acid Hydrochloride | HCID 2796506 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Katalysator | Adams' catalyst | HCID 345198 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | 4-Methylpiperidine-3-carboxylic acid | HCID 13658609 | — |
Reaktionsschritte
AcOH (380 mL) was added to 4-methylnicotinic acid hydrochloride (50.5 g, 291 mmol, Maybridge) and PtO2 (5.05 g, 22.2 mmol, Johnson Matthey) in a 600 mL stainless steel reactor. The mixture was stirred under 220 psi of hydrogen at ambient temperature for about 14 hr. The supernatant solution was filtered through a nylon membrane and rinsed with enough AcOH until only the catalyst remained. The filtrate was concd under reduced pressure to give a clear oil that solidified upon cooling to ambient temperature to give crude 4-methylpiperidine-3-carboxylic acid with AcOH as an excipient (88.94 g, 170% crude): LC/MS (Table 1, Method b) Rt=0.44 min; MS m/z: 144 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08426411B2 |
| Quelldatensatz | uspto-grants-2013_04 |
| ORD ID | ord-38064ad3a6ae4dd8847fe8d2c1fddb7a |
| Quellennotiz | uspto-grants-2013_04 |