HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 66732276, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | HCID 66734932 | HCID 66734932 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 66732276 | HCID 66732276 | 98.3% |
Reaction Steps
Dimethyl 2-(4-fluorophenyl)piperidine-1,4-dicarboxylate (8.97 g, 30.38 mmol) was dissolved in acetonitrile (60 mL) and water (1.200 mL), then lithium bromide (21.10 g, 243.00 mmol) was added. Triethylamine (16.84 mL, 121.50 mmol) was added and the resulting brown suspension was heated under reflux for 1 h. Water (120 mL) and MTBE (120 mL) were added. The organic phase was extracted with water (2×25 mL). The pooled aqueous layer was acidified to pH 1 with 6 M HCl and extracted with MTBE (2×150 mL). The combined organic layer was washed with water (25 mL), dried over anhydrous Na2SO4 and evaporated. 2-(4-Fluorophenyl)-1-(methoxycarbonyl)piperidine-4-carboxylic acid (8.4 g, 98%) was isolated as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08415378B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-c2c1336076e6442ea0233f40000cc1a8 |
| Source note | uspto-grants-2013_04 |