HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244273Generated: October 30, 2026
Sodium Carbonate → 7-Oxa-3-azabicyclo[4.1.0]heptan-3-yl(phenyl)methanone
https://huagongshe.com/reaction/244273
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 3,6-dihydro-2H-pyridin-1-yl(phenyl)methanone | HCID 570037 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Oxa-3-azabicyclo[4.1.0]heptan-3-yl(phenyl)methanone | HCID 332197 | 62.6% |
Reaction Steps
Into a solution of 10 (2.27 g, 12.1 mmol) in CH2Cl2 (20 mL), a solution of 3-chloroperoxybenzoic acid (5.43 g, 77% pure, 24.3 mmol) in CH2Cl2 (40 mL) was added dropwise at 0° C. The reaction mixture was stirred at room temperature for 5 hrs. After the reaction was complete as determined by TLC (hexane/ethyl acetate, 1/1, v/v), saturated Na2CO3 solution (50 mL) was added into the reaction vial slowly with stirring. The reaction mixture was stirred for 30 min. The organic layer was washed with saturated Na2CO3 solution (50 mL×3), brine solution (50 mL), dried over Na2SO4 and concentrated under reduced pressure. The crude product was purified by silica gel column chromatograph using hexane/ethyl acetate (3/1, v/v) as the mobile phase to afford the product as a sticky oil (1.54 g, 62%). 1H NMR (CDCl3): δ 2.04-2.18 (m, 2H), 3.09-4.40 (m, 6H), 7.28-7.47 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658131B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-840461a1af8d40d685e82eccafc25788 |
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| Source note | uspto-grants-2014_02 |
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