HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-tert-Butyl 4-ethyl 5-oxoazepane-1,4-dicarboxylate → HCID 67979385, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-tert-Butyl 4-ethyl 5-oxoazepane-1,4-dicarboxylate | HCID 4436570 | — |
| Reactant | HCID 178418268 | HCID 178418268 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 67979385 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09346816B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-65aa2195e4234d46bfe8b53af75cc179 |
| Source note | uspto-grants-2016_05 |