HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406541Generated: October 30, 2026
Ethanol → Ethyl 4-amino-2-ethoxy-5-nitro-benzoate
https://huagongshe.com/reaction/1406541
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | Ethyl 4-amino-2-fluoro-5-nitrobenzoate | HCID 59529828 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 4-amino-2-ethoxy-5-nitro-benzoate | HCID 67230429 | — |
Reaction Steps
KHMDS (1.92 g, 9.64 mmol) was added to a mixture of ethyl 4-amino-2-fluoro-5-nitro-benzoate (2.00 g, 8.77 mmol) and ethanol (0.56 mL, 9.64 mmol) in 70 mL THF at 0° C. The mixture was stirred at 60° C. for 16 h. Then KHMDS (1.92 g, 9.64 mmol) and ethanol (1.2 mL, 20.7 mmol) were added at ambient temperature and the mixture was stirred at 60° C. for 2 h. 100 mL dichloromethane were added and the mixture extracted with sat. NH4Cl (aq). The organic layer was evaporated, the residue mixed with ethyl acetate, washed with sat. NaCl (aq), dried over Na2SO4, filtered and evaporated. The residue was purified twice by chromatography (silica gel; eluens: petrol ether/ethyl acetate=1:1 and 2:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916599B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-fb248388f9c54bc8ba9663aaa49a0ced |
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| Source note | uspto-grants-2014_12 |
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