HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597971Generated: October 27, 2026
Triethylamine → Ethyl 6-oxo-3-azabicyclo[3.2.1]octane-3-carboxylate ethylene ketal
https://huagongshe.com/reaction/597971
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Azabicyclo[3.2.1]octan-6-one ethylene ketal | HCID 59751989 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 6-oxo-3-azabicyclo[3.2.1]octane-3-carboxylate ethylene ketal | HCID 86602199 | 61.3% |
Reaction Steps
3-Azabicyclo[3.2.1]octan-6-one ethylene ketal (7.69 g, 45.5 mmol) was dissolved in methylene chloride (200 ml) and chilled to 0° C. To this solution was added triethylamine (6.34 ml, 91.0 mmol), then ethyl chloroformate (4.02 ml, 50.1 mmol) drop-wise. The reaction was warmed to ambient temperature and stirred for 18 h. Saturated sodium bicarbonate solution (100 ml) was added, and the organic layer was separated. The aqueous layer was saturated with sodium chloride and extracted with methylene chloride (1×100 ml). The organics were then combined, dried over sodium sulfate, filtered and concentrated. The crude brown residue was then distilled on a Kugelrohr apparatus (0.2 mm Hg, unknown temperature) to yield a clear, dark brown oil (6.72 g, 61.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897611B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-19c0b7c8fe7e4f46919c008d7bd24796 |
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| Source note | uspto-grants-2011_03 |
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