HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → N-[2-(7-oxabicyclo[4.1.0]hept-2-yloxy)phenyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-[2-(2-cyclohexen-1-yloxy)phenyl]acetamide | HCID 22313659 | — |
| Product | N-[2-(7-oxabicyclo[4.1.0]hept-2-yloxy)phenyl]acetamide | HCID 22313696 | 73% |
Reaction Steps
To a solution of N-[2-(2-cyclohexen-1-yloxy)phenyl]acetamide (76 mg, 329 μmol, 1.0 equiv.) in dichloromethane (5 ml) m-chlorobenzoic acid (85 proz.; 121 mg, 559 μmol, 1.7 equiv.) was added at 0° C. Stirring was continued overnight while the reaction mixture was allowed to warm up slowly to room temperature. The heterogenous mixture was diluted with ethyl acetate and washed with sat. sodium sulfite, 5% sodium hydroxide and brine. Drying over sodium sulfate, evaporation of the solvent and flash chromatography on silica gel provided 59 mg (73%) of the title compound as a mixture of the diastereoisomers (ratio A:B=trans:cis=5:3 [1H-NMR]).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06943188B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-84bf286c424f4c6bb6ebb0523246663b |
| Source note | uspto-grants-2005_09 |