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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528713Generated: October 28, 2026

1-tert-Butyl 4-ethyl 5-oxoazepane-1,4-dicarboxylate → HCID 67979385, compound

https://huagongshe.com/reaction/528713

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-tert-Butyl 4-ethyl 5-oxoazepane-1,4-dicarboxylateHCID 4436570—
ReactantHCID 178418268HCID 178418268—
CatalystCupric acetateHCID 8895—
SolventBenzeneHCID 241—
ProductHCID 67979385HCID 67979385—

Reaction Steps

To 4.64 g (16.26 mmol) 5-oxo-azepane-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester (route 1 step a) in 200 mL benzene at room temperature was added 1.47 g (8.13 mmol) copper (II) acetate and the resulting reaction mixture was stirred at room temperature for 30 minutes. 7.21 g (16.26 mmol) lead (IV) tetraacetate was added and the reaction was stirred at room temperature for 3 hours. After evaporation of the solvent, the material was partitioned between 250 mL EtOAc and 150 mL H2O, the organic layer was separated and washed with H2O (150 mL) and saturated brine (150 mL) and dried over MgSO4. After filtration and evaporation of the solvent the resulting solid was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346816B2
Source datasetuspto-grants-2016_05
ORD IDord-65aa2195e4234d46bfe8b53af75cc179
Source noteuspto-grants-2016_05