HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-butyl 3-(2-methoxyethenyl)-1-piperidinecarboxylate → tert-Butyl 3-(2-oxoethyl)piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-butyl 3-(2-methoxyethenyl)-1-piperidinecarboxylate | HCID 69249758 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | tert-Butyl 3-(2-oxoethyl)piperidine-1-carboxylate | HCID 22258947 | 60% |
Reaction Steps
tert-Butyl 3-(2-methoxyethenyl)-1-piperidinecarboxylate (1.16 g, 4.81 mmol) was dissolved in 90% formic acid (2 mL). The mixture was stiffed at room temperature for 40 min. The mixture was then partitioned between ethyl acetate and saturated aqueous NaHCO3 solution. The separated organic phase was washed with brine, dried over Na2SO4, filtered and evaporated. Purification by column chromatography (hexane/ethyl acetate=4/1) gave tert-butyl 3-(2-oxoethyl)-1-piperidinecarboxylate as a colorless oil (652 mg, yield; 60%). [Starting Compound 2H]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07232909B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-4d6a3f7440d44da0940eeac6a7c366f5 |
| Source note | uspto-grants-2007_06 |