HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 66731973, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | Dimethyl 2-(2,4-difluorophenyl)piperidine-1,4-dicarboxylate | HCID 66734584 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 66731973 | HCID 66731973 | — |
Reaction Steps
Dimethyl 2-(2,4-difluorophenyl)piperidine-1,4-dicarboxylate (2.38 g, 7.60 mmol) was dissolved into acetonitrile (35 mL) and water (0.700 mL), then lithium bromide (5.28 g, 60.77 mmol) was added. Et3N (4.24 mL, 30.39 mmol) was added and the resulting yellow suspension was heated under reflux for 2 h. Water (50 mL) and MTBE (150 mL) were added. The phases were separated and the organic layer was extracted with water (2 times). The pooled water layers were acidified to pH 1 with 3.8 M HCl and extracted with MTBE (2 times). The combined organic layer was dried over Na2SO4, filtered and evaporated yielding 2-(2,4-difluorophenyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid (2.27, quant.) as a slightly yellow semi-solid. MS m/z 300 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08415378B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-01197308a24b43f8b805a51b36669c8a |
| Source note | uspto-grants-2013_04 |