HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → cis-1-Tert-butyl 3-ethyl 4-methylpiperidine-1,3-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | Ethyl 4-methylpiperidine-3-carboxylate | HCID 13658603 | — |
| Reactant | 1-Tert-butyl 3-ethyl 4-methylpiperidine-1,3-dicarboxylate | HCID 70791601 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | cis-1-Tert-butyl 3-ethyl 4-methylpiperidine-1,3-dicarboxylate | HCID 131735164 | 83.3% |
Reaction Steps
Di-tert-butyl dicarbonate (3.26 g, 15.20 mmol) was added to a solution of ethyl 4-methylpiperidine-3-carboxylate (2.0 g, 11.68 mmol) and triethylamine (3.9 mL, 28.05 mmol) in anhydrous dichloromethane (50 mL) at 0° C. The reaction mixture was stirred at room temperature for 18 h. The mixture partitioned between dichloromethane and water. The organics were dried over sodium sulfate, filtered and concentrated under reduced pressure to afford a mixture of the cis and trans diastereomers of 1-tert-butyl 3-ethyl 4-methylpiperidine-1,3-dicarboxylate (3.0 g). The crude material was purified via column chromatography (5-10% ethyl acetate in petroleum ether) to afford cis-1-tert-butyl 3-ethyl 4-methylpiperidine-1,3-dicarboxylate (2.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296745B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-4a634299e5f74e8d8bc683344d04df11 |
| Source note | uspto-grants-2016_03 |