HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369975Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 71226801, compound
https://huagongshe.com/reaction/2369975
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sulfur trioxide-pyridine | HCID 168533 | — |
| Reactant | HCID 71227178 | HCID 71227178 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71226801 | HCID 71226801 | 54% |
Reaction Steps
To a round bottom flask was added 2-(4-nitrophenyl)-2-azabicyclo[2.2.1]heptan-6-ol (150 mg, 0.640 mmol), Et3N (0.446 mL, 3.20 mmol) and CH2Cl2 (3 mL). The reaction was cooled to 0° C. Pyridine sulfur trioxide (510 mg, 3.20 mmol) and DMSO (0.909 mL, 12.81 mmol) were mixed in a vial until the solution turned clear and then this clear solution was added to the reaction mixture at 0° C. The reaction was slowly warmed to rt and stirred at rt for 2 hrs. The reaction was diluted with CH2Cl2 (25 ml). The organic solution was washed with water (2×20 ml) and saturated aqueous NaCl (20 ml). The organic layer was dried with MgSO4, filtered and concentrated. The resulting residue was purified using silica gel chromatography (ISCO system) eluting with a gradient of 0-100% EtOAc/Hex to give the product, 2-(4-nitrophenyl)-2-azabicyclo[2.2.1]heptan-6-one, (80 mg, 0.344 mmol, 54% yield) as a yellow solid. Anal. Calcd. for C12H12N2O3 m/z 232.2, found: 233.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710049B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-032e3fc748bc43b4b7c98729e8771593 |
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| Source note | uspto-grants-2014_04 |
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