HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(2,4-Difluorobenzyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | Dimethyl 2-(2,4-difluorobenzyl)piperidine-1,4-dicarboxylate | HCID 66734674 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(2,4-Difluorobenzyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid | HCID 66732471 | 92% |
Reaction Steps
To a suspension of lithium bromide (18.06 g, 207.99 mmol) in acetonitrile (80 mL) and water (1.6 mL) was added triethylamine (14.42 mL, 104.00 mmol) followed by dimethyl 2-(2,4-difluorobenzyl)piperidine-1,4-dicarboxylate (8.51 g, 26.00 mmol) in acetonitrile (40 mL). The resulting mixture was heated under reflux for 2 h 30 min, then cooled to room temperature and water and MTBE were added. The organic phase was extracted with water twice. The pooled aqueous layers were adjusted to pH 1 with 3.8 M HCl and then extracted with DCM (3×). The combined organic layers were dried over MgSO4 and evaporated to yield 2-(2,4-difluorobenzyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid (7.48 g, 92%) as an orange solid. MS m/z 314 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08415378B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-91e53096c4f148919f3b3842311204a1 |
| Source note | uspto-grants-2013_04 |