HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Benzyl-6-oxa-3-azabicyclo(3.1.0)hexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 12153330 | HCID 12153330 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-Benzyl-6-oxa-3-azabicyclo(3.1.0)hexane | HCID 9815370 | 77% |
Reaction Steps
To an ice-cooled solution of 1-benzyl pyrroline (0.01 mol), 98% H2SO4 (0.012 mol), water (1.5 g), and acetone (10 mL) in a round bottom flask was added 77% m-CPBA (0.013 mol) with stirring, and allowed to react for about 50 h at room temperature. After completion of the reaction (TLC monitor), acetone was evaporated under reduced pressure, and the mixture was neutralized by 1M NaOH, and extracted with toluene (30 mL×3). The precipitates that appeared were filtered, and the filtrate was repeatedly washed with water (30 mL×2). After the solvent was evaporated under reduced pressure, pure product was obtained in 77% yield via column chromatography (silica gel, CH2Cl2:EtOAc:MeOH, 7.5:2.00:0.5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07994326B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-8fed5314886d47b5bf1cdfec0d9be62f |
| Source note | uspto-grants-2011_08 |