HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055628Generated: November 1, 2026
Dichloromethane → 5,6-Epoxy-2-norbornanesulfonamide
https://huagongshe.com/reaction/1055628
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Bicyclo[2.2.1]hept-5-ene-2-sulfonamide | HCID 22094258 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5,6-Epoxy-2-norbornanesulfonamide | HCID 45080601 | 63.1% |
Reaction Steps
To a four-necked flask having an inner volume of 500 ml and equipped with an electromagnetic stirring device, a nitrogen inlet tube, and a thermometer, there were charged 10.0 g (57.7 mmol) of 5-norbornene-2-sulfonamide, 15.1 g (180.0 mmol) of sodium bicarbonate, and 200 g of dichloromethane. After cooling the mixture to 5° C., 14.8 g (60.0 mmol) of 70% m-chloroperbenzoic acid was added thereto over a 20 minute period, and the mixture was stirred at 5° C. for 2 hours. To the reaction mixture was added 100 g of distilled water, and the mixture was separated into an organic layer and an aqueous layer. The organic layer was washed with 40 g of distilled water and concentrated under reduced pressure. By recrystallizing the residue obtained from ethyl acetate, there was obtained 6.89 g (36.4 mmol) of 5,6-epoxy-2-norbornanesulfonamide represented by the following formula (yield 63%):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09395625B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-8269be94461546c8884137fefd17ec64 |
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| Source note | uspto-grants-2016_07 |
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