HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(3,4-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-(3,4-difluorobenzyl)piperidine-1,4-dicarboxylate | HCID 66734915 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(3,4-Difluorobenzyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid | HCID 66731819 | 99% |
Reaction Steps
Dimethyl 2-(3,4-difluorobenzyl)piperidine-1,4-dicarboxylate (7.010 g, 21.42 mmol) was dissolved in acetonitrile (75 mL) and water (1.5 mL). Lithium bromide (14.88 g, 171.33 mmol) and triethylamine (11.87 mL, 85.66 mmol) were added and the resulting yellow suspension was heated at reflux for 3 h. Water (100 mL) and MTBE (300 mL) were added. The organic phase was extracted with water (×2). The pooled aqueous layer was acidified to pH 1 with 3.8 M HCl and then extracted with MTBE (×2). The combined organic layer was washed with water, dried over Na2SO4, filtered and evaporated to yield 2-(3,4-difluorobenzyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid (6.62 g, 99%) as a yellow 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-1bfb74ea3879453b8687dfec779a5a5a |
| Source note | uspto-grants-2013_04 |