HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Benzyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 1,2,3,6-Tetrahydropyridine-1-carboxylate | HCID 21691317 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate | HCID 13186888 | 99% |
Reaction Steps
3-Chlorobenzoperoxoic acid (51.1 g, 228 mmol) was added portion wise to a solution of 5,6-dihydropyridine-1(2H)-carboxylate (33.0 g, 152 mmol) in DCM (200 mL) at 0° C. After 10 minutes at 0° C., the reaction was warmed to room temperature and stirred at room temperature for 4 hours. The reaction mixture was diluted with ether (800 mL), washed with 1N NaOH solution (2×200 mL), saturated N2SO3 solution (2×100 mL), brine (100 mL), dried (sodium sulfate) and concentrated in vacuo to give benzyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate (35.0 g, 99%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08981085B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-16f2a456716b4fec909d5b096320abbd |
| Source note | uspto-grants-2015_03 |