HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435848Generated: November 1, 2026
Ethyl bromoacetate → ethyl 2-(4-formyl-2-nitrophenoxy)acetate
https://huagongshe.com/reaction/1435848
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Hydroxy-3-nitrobenzaldehyde | HCID 18169 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl 2-(4-formyl-2-nitrophenoxy)acetate | HCID 5305379 | — |
Reaction Steps
A solution of 4-hydroxy-3-nitrobenzaldehyde (6.9 g) and ethyl bromoacetate (5.0 mL) in dimethylformamide (250 mL) was treated with anhydrous potassium carbonate (10 g) and the mixture was heated at 60° C. for 18 hours and evaporated to dryness. The residue was partitioned between water and diethyl ether, and the diethyl ether layer was washed with 0.5M sodium hydroxide. It was then dried over anhydrous sodium sulfate and evaporated to give an oil that was chromatographed on silica gel (ethyl acetate/dichloromethane) to afford an oil (1.9 g). MS (+ve ion electrospray) m/e 253 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07618959B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-7e40c1c1eb6b497e8956bab2d8bdc99f |
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| Source note | uspto-grants-2009_11 |
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