HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978012Generated: October 29, 2026
Potassium Carbonate → Ethyl 4-((3-formyl-4-nitrophenyl)oxy)butyrate
https://huagongshe.com/reaction/978012
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Hydroxy-2-nitrobenzaldehyde | HCID 39211 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 4-((3-formyl-4-nitrophenyl)oxy)butyrate | HCID 10588876 | — |
Reaction Steps
To a solution of 5-hydroxy-2-nitrobenzaldehyde (84.0 g) and ethyl 4-bromobutyrate (86 ml) in dry dimethylformamide (500 ml) blanketed under dry nitrogen was added potassium carbonate (76.0 g). The reaction mixture was heated to 100° C. for 1 hour. This mixture was cooled, and the solvent removed by evaporation to give a dark brown syrup. This residue was partitioned between ethyl acetate and saturated sodium carbonate (500 ml each). The organic layer was washed with additional saturated sodium carbonate (3×500 ml), and with brine (2×500 ml), dried, filtered and evaporated to give a dark brown syrup. Kugelrohr distillation (180° C., 0.2 mm) afforded ethyl 4-((3-formyl-4-nitrophenyl)oxy)butyrate (95 g) as a bright yellow syrup which slowly darkened upon standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04663320 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-0ac900917af346058191ccb4304e52e0 |
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| Source note | uspto-grants-1987_05 |
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