HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963289Generated: October 30, 2026
HCID 66731807, compound → HCID 66732323, compound
https://huagongshe.com/reaction/1963289
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66731807 | HCID 66731807 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 66732323 | HCID 66732323 | 89.2% |
Reaction Steps
Methyl 2-(2-(trifluoromethyl)benzyl)isonicotinate (4.613 g, 15.62 mmol) was dissolved in acetic acid (40 mL) and platinum(IV) oxide (0.26 g, 1.14 mmol) added. The resulting mixture was hydrogenated in a Büchi hydrogenator for 3 h at room temperature and 5 bar. More platinum(IV) oxide (160 mg) was added and the hydrogenation continued at room temperature at 5 bar for 2 h. The catalyst was filtered off and washed with MeOH and the eluate evaporated. DCM and 10% K2CO3 were added and the phases separated. The water phase was extracted with DCM and the combined organic phase washed with water, passed through a phase separator and evaporated to yield methyl 2-(2-(trifluoromethyl)benzyl)-piperidine-4-carboxylate (4.20 g, 89%) as a yellow oil. MS m/z 302 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08415378B2 |
|---|
| Source dataset | uspto-grants-2013_04 |
|---|
| ORD ID | ord-f13376e069a34f31ae9953fc613d8e20 |
|---|
| Source note | uspto-grants-2013_04 |
|---|