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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353047Generated: October 31, 2026

Boron trifluoride etherate → Diethyl 5-oxoazepane-1,4-dicarboxylate

https://huagongshe.com/reaction/2353047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantEthyl 4-oxo-1-piperidinecarboxylateHCID 34767—
ReactantEthyl diazodicarboxylateHCID 86610729—
SolventDiethyl EtherHCID 3283—
ProductDiethyl 5-oxoazepane-1,4-dicarboxylateHCID 12485293—

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a cold solution (−30° C.) of 1-carbethoxypiperidin-4-one (3.0 ml, 26.5 mmol) in anhydrous ether, were simultaneously added a solution of boron trifluoride etherate (3.4 ml, 26.5 mmol) in diethyl ether (2.8 ml) and a solution of ethyl diazodicarboxylate (3.6 ml, 34.5 mmol) in diethyl ether (2.8 ml) over 1.5 hours via a syringe-pump. Upon completion of additions, the reaction mixture was allowed to stir for an additional hour at −30° C. and then warmed to room temperature. The reaction mixture was washed with 30% potassium carbonate and the organic phase was dried over Na2SO4 and concentrated in vacuo to give diethyl 5-oxoazepane-1,4-dicarboxylate as a crude yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07749994B2
Source datasetuspto-grants-2010_07
ORD IDord-7b69eb52042141b5b90c6e0f25005880
Source noteuspto-grants-2010_07