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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Azabicyclo[3.2.1]octan-6-one ethylene ketalHCID 59751989—
SolventDichloromethaneHCID 6344—
ProductEthyl 6-oxo-3-azabicyclo[3.2.1]octane-3-carboxylate ethylene ketalHCID 8660219961.3%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897611B2
Source datasetuspto-grants-2011_03
ORD IDord-19c0b7c8fe7e4f46919c008d7bd24796
Source noteuspto-grants-2011_03