Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | 3-Bromo-1-(2-methoxy-4-nitrophenyl)pyridin-2(1H)-one | HCID 59410145 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86683907 | HCID 86683907 | — |
Reaction Steps
39.3 g of sodium tert-butylate (0.41 mol) were introduced as initial charge in 300 ml of dioxane, and 65.5 g of diethyl malonate (0.41 mol) were added dropwise over the course of 15 min such that the temperature does not exceed 30° C. After 1 h, 2.70 g (8.8 mmol) of bis(2-pyridinecarboxylato)copper(II) complex and 38.0 g (0.12 mol) of 3-bromo-1-(2-methoxy-4-nitrophenyl)pyridin-2(1H)-one were added and the reaction mixture was heated at reflux for 8 h. After cooling to RT, the mixture was further stirred overnight. The reaction mixture was filtered off from the solid with suction, the residue was after-washed with dioxane and the combined organic fractions were evaporated to ca. 300 g on a rotary evaporator. The crude solution was used in the next stage without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802860B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-9a0f2215438f439289c528eadb07a08d |
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| Source note | uspto-grants-2014_08 |
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