Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Reactant | 2-Azabicyclo(2.2.1)hept-5-en-3-one | HCID 548678 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22673287 | HCID 22673287 | 76% |
Reaction Steps
45.1 g of (±)-2-azabicyclo[2.2.1]hept-5-en-3-one were dissolved in acetonitrile (310 ml) and pyridine (39 ml) under nitrogen. At 10° C., 54.1 g of isobutyryl chloride were added dropwise over the course of 1 h. The reaction was then stirred at room temperature for 5 h. 140 ml of water were added to the mixture, and the acetonitrile was evaporated off in vacuo. The aqueous phase was extracted with 4×120 ml of ethyl acetate. The combined organic phases were washed with 1N HCl (50 ml), saturated NaHCO3 (50 ml) and NaCl (50 ml) solutions, dried with sodium sulphate and completely evaporated. The residue was boiled under reflux in n-hexane (240 ml) with active charcoal. After filtration of the active charcoal, the filtrate was cooled to 0° C. and the title compound was filtered. 54.5 g of produce were obtained. The yield was 76%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06252112B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-22470767f5e54f5bbb4ccb0742e20f34 |
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| Source note | uspto-grants-2001_06 |
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