HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76455Generated: October 28, 2026
3-Nitrophenol → Diethyl 2-methyl-2-(3-nitrophenoxy)malonate
https://huagongshe.com/reaction/76455
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Nitrophenol | HCID 11137 | — |
| Reactant | Diethyl bromomethylmalonate | HCID 94944 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diethyl 2-methyl-2-(3-nitrophenoxy)malonate | HCID 22060402 | 80% |
Reaction Steps
Diethyl 2-bromo-2-methylmalonate (1.0 g, 3.95 mmole) was added to a stirred suspension of potassium fluoride (0.57 g, 9.8 mmole) in dry DMF (5 mL). After stirring for 20 min at room temperature, 3-nitrophenol (0.55 g, 3.95 mmole) was added. The resulting mixture was stirred at 60° C. for 6 h, cooled to room temperature, diluted with water (30 mL) and extracted with ethyl acetate (3×200 mL). The organic layer was washed with aq. 1N NaOH (2×75 mL), dried over anhydrous Na2SO4, filtered and evaporated in vacuo to provide diethyl 2-methyl-2-(3-nitrophenoxy)malonate (0.89 g, 80%). 1H NMR (CDCl3): δ 7.92 (dd, 1H, J=2.3 and 8.2 Hz), 7.82 (t, 1H, J=2.3 Hz), 7.41 (t, 1H, J=8.2 Hz), 7.30 (dd, 1H, J=2.3 and 8.2 Hz), 4.28 (qt, 4H, J=7.0 Hz), 1.81 (s, 3H), 1.26 (t, 6H, J=7.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835430B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-e0c767dbf25c42a995a6affc2f40bf2c |
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| Source note | uspto-grants-2014_09 |
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