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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528707Generated: October 25, 2026

Boron trifluoride etherate → 1-tert-Butyl 4-ethyl 5-oxoazepane-1,4-dicarboxylate

https://huagongshe.com/reaction/528707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl diazoacetateHCID 12192—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
SolventDiethyl EtherHCID 3283—
Product1-tert-Butyl 4-ethyl 5-oxoazepane-1,4-dicarboxylateHCID 4436570—

Reaction Steps

To 10.0 g (50.18 mmol) 4-oxo-piperidine-1-carboxylic acid tert-butyl ester in 60 mL anhydrous ether maintained between −25° C. and −30° C. were added, over 20 minutes, solutions of 8.2 mL (65.23 mmol) boron trifluoride diethyl etherate in 17 mL anhydrous ether, followed by 6.85 mL (65.23 mmol) ethyl diazoacetate in 17 mL anhydrous ether, and the reaction was maintained between −25° C. and −30° C. for 1 hour. The mixture was allowed to warm to room temperature, 30 mL 30% potassium carbonate solution was added and the mixture extracted with EtOAc (3×30 mL), the organic layers were combined and dried with MgSO4. After filtration, the solvent was evaporated to give the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346816B2
Source datasetuspto-grants-2016_05
ORD IDord-20eb548a9b5b4a9298944ceafbfd18e6
Source noteuspto-grants-2016_05