HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(4-Fluorophenethyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | Dimethyl 2-(4-fluorophenethyl)piperidine-1,4-dicarboxylate | HCID 86646603 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 2-(4-Fluorophenethyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid | HCID 66732483 | 143.7% |
Reaction Steps
Dimethyl 2-(4-fluorophenethyl)piperidine-1,4-dicarboxylate (3.18 g, 9.83 mmol) was dissolved in acetonitrile (35 mL) and water (0.7 mL) and lithium bromide (6.83 g, 78.67 mmol) was added. Triethylamine (5.45 mL, 39.34 mmol) was added and the resulting suspension was heated under reflux for 5 h. MTBE and water were added, the phases separated and the organic layer was extracted with water. The combined aqueous layers were acidified to pH 1 with 3.8 M HCl and extracted with MTBE. The combined organic layers were washed with water, dried with Na2SO4 and evaporated. Crude 2-(4-fluorophenethyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid (4.37 g) was isolated. MS m/z 310 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08415378B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-3cad11dcf3e94f9a954b52bd743903db |
| Source note | uspto-grants-2013_04 |